{"jobs":[{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5140170007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4585997007,"location":{"name":"San Diego, California, United States"},"metadata":null,"id":5140170007,"updated_at":"2026-05-28T19:07:46-04:00","requisition_id":"735","title":"Associate Director/Director, Drug Safety \u0026 Pharmacovigilance (Quality \u0026 Compliance)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-18T12:14:28-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director/ Director of Drug Safety \u0026amp;amp; Pharmacovigilance (PV) Quality \u0026amp;amp; Compliance, is a key role and is responsible for oversight of Drug Safety \u0026amp;amp; PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program within the Drug Safety \u0026amp;amp; Pharmacovigilance department. This position will lead preparation, delivery, and response to GVP inspections, work closely with QA to ensure Patient Safety input to GCP, GVP, GMP inspections, support issue reporting and CAPA development, monitor quality and compliance. The successful candidate will provide strategic direction, manage a team of PV Quality \u0026amp;amp; Compliance professionals as applicable, and collaborate with cross-functional teams to enhance the safety and quality of pharmaceutical products.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic guidance and leadership to the pharmacovigilance quality assurance team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement a comprehensive quality assurance strategy aligned with organizational goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop/oversee execution of (end-to-end) PV QA processes and systems to ensure compliance/alignment with regulatory requirements and internal policies/procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively provide Good Pharmacovigilance Practice (GVP) support for clinical, post marketing and commercial activities including PV/ safety systems to protect patient safety and well-being, maintain data integrity, and support implementation of Quality Systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor industry trends, regulatory changes, and best practices to ensure continuous improvement of quality assurance processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor vendor key performance indicator (KPI) metrics and implement measures to enhance the quality of CROs and vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the development, review, and maintenance of Standard Operating Procedures (SOPs) for pharmacovigilance quality assurance activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that SOPs are consistent with current regulations, guidelines, and industry standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage a team of quality assurance professionals, including training, mentoring, and performance evaluations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a collaborative and high-performance work environment to achieve departmental objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct regular internal audits of pharmacovigilance processes, systems, and data to ensure compliance with regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with internal audit teams and external partners during regulatory inspections and audits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement key quality metrics to assess the effectiveness of pharmacovigilance processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present quality assurance reports to senior management, highlighting trends, issues, and opportunities for improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams to assess and manage risks related to pharmacovigilance activities. Identify areas of potential risk and implement strategies to mitigate them proactively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous improvement initiatives to enhance the efficiency and effectiveness of pharmacovigilance quality assurance activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Regularly assess quality and compliance initiatives for effectiveness, outcomes, and relevance, and adjust strategy as needed based on results, risks, and feedback.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with stakeholders to solicit feedback and implement process enhancements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor regulatory intelligence and surveillance activities for emerging regulations in any geography that may impact PV system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee corrective and preventative actions (CAPA) development, execution, closure and, as needed, escalation for CAPAs associated or impacting pharmacovigilance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to drug safety and pharmacovigilance issue management to support early issue detection, CAPA development and completion tracking, and effectiveness assessment for PV systems.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8 years of experience in pharmacovigilance or drug safety, with 6 years in a quality assurance or compliance role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s Degree in a related scientific field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of global pharmacovigilance regulations, guidelines, and industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience in leading and managing teams, including demonstrated leadership skills and the ability to mentor and develop staff.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills, both written and verbal, with the ability to interact effectively with cross-functional teams and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented with strong analytical and problem-solving capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in conducting internal audits and managing regulatory inspections is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in using pharmacovigilance databases and software.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in pharmacy, life sciences, or a related field\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$180,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$230,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4010356007,"name":"Clinical Safety \u0026 Pharmacovigilance","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5037727007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4585997007,"location":{"name":"San Diego, California, United States"},"metadata":null,"id":5037727007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"735","title":"Associate Director/Director, Quality \u0026 Compliance (Drug Safety \u0026 Pharmacovigilance)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-02-04T19:59:52-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director/ Director of Drug Safety \u0026amp;amp; Pharmacovigilance (PV) Quality \u0026amp;amp; Compliance, is a key role and is responsible for oversight of Drug Safety \u0026amp;amp; PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program within the Drug Safety \u0026amp;amp; Pharmacovigilance department. This position will lead preparation, delivery, and response to GVP inspections, work closely with QA to ensure Patient Safety input to GCP, GVP, GMP inspections, support issue reporting and CAPA development, monitor quality and compliance. The successful candidate will provide strategic direction, manage a team of PV Quality \u0026amp;amp; Compliance professionals as applicable, and collaborate with cross-functional teams to enhance the safety and quality of pharmaceutical products.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic guidance and leadership to the pharmacovigilance quality assurance team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement a comprehensive quality assurance strategy aligned with organizational goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop/oversee execution of (end-to-end) PV QA processes and systems to ensure compliance/alignment with regulatory requirements and internal policies/procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively provide Good Pharmacovigilance Practice (GVP) support for clinical, post marketing and commercial activities including PV/ safety systems to protect patient safety and well-being, maintain data integrity, and support implementation of Quality Systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor industry trends, regulatory changes, and best practices to ensure continuous improvement of quality assurance processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor vendor key performance indicator (KPI) metrics and implement measures to enhance the quality of CROs and vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the development, review, and maintenance of Standard Operating Procedures (SOPs) for pharmacovigilance quality assurance activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that SOPs are consistent with current regulations, guidelines, and industry standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage a team of quality assurance professionals, including training, mentoring, and performance evaluations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a collaborative and high-performance work environment to achieve departmental objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct regular internal audits of pharmacovigilance processes, systems, and data to ensure compliance with regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with internal audit teams and external partners during regulatory inspections and audits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement key quality metrics to assess the effectiveness of pharmacovigilance processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present quality assurance reports to senior management, highlighting trends, issues, and opportunities for improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams to assess and manage risks related to pharmacovigilance activities. Identify areas of potential risk and implement strategies to mitigate them proactively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous improvement initiatives to enhance the efficiency and effectiveness of pharmacovigilance quality assurance activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Regularly assess quality and compliance initiatives for effectiveness, outcomes, and relevance, and adjust strategy as needed based on results, risks, and feedback.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with stakeholders to solicit feedback and implement process enhancements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor regulatory intelligence and surveillance activities for emerging regulations in any geography that may impact PV system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee corrective and preventative actions (CAPA) development, execution, closure and, as needed, escalation for CAPAs associated or impacting pharmacovigilance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to drug safety and pharmacovigilance issue management to support early issue detection, CAPA development and completion tracking, and effectiveness assessment for PV systems.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10 years of experience in pharmacovigilance or drug safety, with 9-10 years in a quality assurance or compliance role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s Degree in a related scientific field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of global pharmacovigilance regulations, guidelines, and industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience in leading and managing teams, including demonstrated leadership skills and the ability to mentor and develop staff.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills, both written and verbal, with the ability to interact effectively with cross-functional teams and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented with strong analytical and problem-solving capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in conducting internal audits and managing regulatory inspections is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in using pharmacovigilance databases and software.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in pharmacy, life sciences, or a related field\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$180,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$230,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4010356007,"name":"Clinical Safety \u0026 Pharmacovigilance","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5067834007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4599922007,"location":{"name":"San Diego, California, United States"},"metadata":null,"id":5067834007,"updated_at":"2026-05-28T19:06:58-04:00","requisition_id":"779","title":"Associate Director, Drug Safety Operations","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-03T12:13:25-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Drug Safety Operations will be responsible for maintaining Arrowhead’s safety database, supporting vendor oversight activities, ensuring compliance and operational aspects of PV related activities. The Associate Director, Drug Safety Operations will also support in preparation and review of regulatory reports such periodic aggregate reports in compliance with FDA, EMA and other international guidelines and regulations for clinical programs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support Case Processing and support safety medical review, generate appropriate queries to contact drug safety vendors (CROs) to complete and clarify SAE case information as needed and work with CRO to determine when cases are complete and ready to close.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with clinical and safety teams to support consistent, accurate, and regulatory‑compliant assessment and documentation of SAEs and events of special interest (e.g., pregnancy, overdose) across clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross‑functional stakeholders to support standardized safety set‑up for new clinical studies, including contribution to Safety Management Plans, Safety Monitoring Plans, Clinical Risk Management Plans, and safety system configurations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with CROs and PV vendors to provide oversight of safety case management activities, including quality review processes and monitoring of expedited and aggregate reporting timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Finance, Clinical Operations, and vendors to provide oversight of safety budgets and financial activities, including scope alignment, forecasting, invoice review, and cost tracking.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with internal teams and external partners to manage Pharmacovigilance Agreements (PVAs), SDEAs, and vendor contracts, supporting compliance with regulatory, contractual, quality, and financial requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with safety vendors and CROs to monitor deliverables, support reconciliation processes, maintain TMF/eTMF safety documentation, and promote continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with Clinical Operations, CROs, and PV vendors to support and oversee Clinical–Safety Database reconciliation activities, ensuring timely, accurate, and well‑documented reconciliation across studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work in partnership with Safety Science and Medical teams to support safety surveillance activities, including signal detection, trend analysis, similar‑event evaluations, and review of abnormal laboratory data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Regulatory Affairs and study teams to support safety reporting activities across clinical trials, including preparation for expedited reporting and health authority communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with safety systems and vendor teams to support oversight of the Safety Database (e.g., Argus), including UAT, system updates, data outputs for DSURs, IBs, DSMB/DSC materials, and business continuity activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support inspection readiness and regulatory inspection activities by collaborating on document preparation, reconciliation support, inspection responses, and participation in health authority inspections as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the authoring, review, and maintenance of SOPs, work instructions, and cross‑functional documents, while supporting team development and the Head of Clinical Safety \u0026amp;amp; Pharmacovigilance in governance activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support activities related to implementing and maintaining the Safety Database, supporting ARGUS activities, Overseeing the Safety Vendors, and coordinating the Safety Reporting from Clinical Trials and Collaborators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support other members of Safety Operations and Science personnel and ensure flawless execution of Safety and Pharmacovigilance processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in tracking/monitoring of cases and other vendor or partner deliverables to ensure quality and timeliness of safety management activities, as well as adherence to regulatory and contractual obligations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide drug safety case management support to Safety medical monitors; assist in following up on queries for case reports, abnormal laboratory values, or any other relevant safety and medical data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support reviewing and monitoring of SAE/SUSAR case processing including, performing the secondary quality review for all case reports in the safety\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor SAE reconciliation with the Arrowhead PV vendor and study CRO to ensure the reconciliation process is occurring for all clinical studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support monitoring safety surveillance for Arrowhead\u0026#39;s clinical development products to ensure corporate compliance with national and international adverse event reporting requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in the production and validation of appropriate safety data output from the external or internal safety database for required safety deliverables (e.g. DSUR, IB, ad hoc analyses etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with periodic Disaster recovery and Business continuity tests as needed with Safety Database.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Drug Safety team with listings and data from the Argus database.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8 years of experience in Drug Safety/Pharmacovigilance Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor of Science/4-year degree in Biological or Life Sciences, pharmacy, nursing or related healthcare field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of case management and processing. Experience in using ARGUS or other safety databases. Experience with MedDRA/WHO for coding AEs, medical history, and concomitant medications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with preparation with aggregate reports, preferably for investigational drugs (i.e., DSURs, IND Annual reports) or post-marketing products (i.e., PSUR/PBRER, PADERs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working experience with Safety Databases (Argus, ArisG or other) is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of ICH E2B guidelines in clinical and post-marketing studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good organizational skills with the ability to perform multiple tasks efficiently and effectively.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;HCP experience\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$170,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$200,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4010356007,"name":"Clinical Safety \u0026 Pharmacovigilance","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5148894007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4637888007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5148894007,"updated_at":"2026-05-28T11:58:49-04:00","requisition_id":"874","title":"Associate Engineer II, Automation","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-28T11:58:49-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Engineer II, Automation, plays a critical role in plant engineering operations and contributes to continuous improvements to enhance efficiency, safety, and productivity for the manufacturing plant. The Associate Automation Engineer II is responsible for supporting the lifecycle of our process control programming, hardware, and supporting network infrastructure under the guidance of management and subject matter experts. Core duties will include implementing efficiency/safety/process automation improvements, providing technical support to the Plant Operations team, and participating in projects to transfer new automated equipment to manufacturing facilities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities \u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Program, troubleshoot, and maintain PLC and SCADA programs and process control hardware to support pharmaceutical manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot simple to moderate automation and associated electrical and mechanical system issues with support from subject matter experts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently identify and complete simple controls and equipment corrective actions or work as part of team to identify root cause and correct moderate to complex electrical, controls, and mechanical issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define scope and deliverables of automation improvement projects of simple to moderate complexity; lead or work as part of a cross functional team to plan, implement and test improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate on project teams to implement moderate to complex automation projects; collaborate on shared deliverables, mitigate project risks, provide project updates, and meet timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and coordinate with contracted system integrators with project delivery as part of a cross functional project team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Update and maintain engineering documents, electrical / network drawings, and equipment records with changes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advance standard operating procedures (SOPs) for process control system administration, maintenance, and management of changes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently as a super user for simple automation systems, such as Environmental Monitoring. Perform routine administrative level tasks such as new device addition, user addition and review, and alarm strategy review with end user input.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute process control system administrative and maintenance tasks such as hardware and software version reviews, back-up and patching in adherence to prescribed schedule and procedures. \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with IS\u0026amp;amp;I to troubleshoot process control system network infrastructure and hardware.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all automation activities comply with internal and external compliance requirements by following good engineering practices and change management procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide front line troubleshooting of process automation programming and hardware issues to support business continuity. Provide second level troubleshooting to maintenance departments for process control instrumentation and wiring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a point of contact and escalation for colleagues in Metrology, Process Engineering, and IS\u0026amp;amp;I for automation needs and issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Engineering (Chemical, Mechanical, Electrical) or similar field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 3+ years of experience in an Automation Engineering role\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with PLC (Programmable Logic Controller) and/or SCADA (Supervisory Control and Data Acquisition) programming\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Growing understanding of FDA compliance requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Awareness of cGMP / GAMP automation requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing communication and interpersonal skills, with the ability to participate on cross-functional\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing technical writing skills with high attention to\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work with management to prioritize timelines and deadlines across assignments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with SIEMENS process control hardware and programming (STEP 7, WinCC, Process Historian) systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with commissioning, qualification, and change management in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledgeable in process control instrumentation troubleshooting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands on experience with process equipment operations, mechanical integration with control systems, and mechanical troubleshooting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience using CAD software for updating electrical and automation drawings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of process control network infrastructure, troubleshooting, and administration.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$75,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$90,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5103533007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4616109007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5103533007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"833","title":"Associate Manufacturing Scientist I (2nd shift)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-09T08:44:34-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Manufacturing Scientist I (second shift) role\u0026amp;nbsp;will involve assisting in the synthesis and subsequent purification steps of\u0026amp;nbsp;large scale oligonucleotides. The operator must comply with GLP/GMP protocols and\u0026amp;nbsp;be able to follow all association SOPs and work instructions when performing and\u0026amp;nbsp;documenting operations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2\u0026lt;sup\u0026gt;nd\u0026lt;/sup\u0026gt; shift work hours are 1pm – 11:30 pm Monday - Thursday and includes a 10% shift differential.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Follow batch records, SOPs, and work instructions to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document all operations in batch records and logbooks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comply with GMP protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operate large scale oligonucleotide manufacturing equipment (i.e. oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist other chemists within the Manufacturing group during synthesis and purification of oligonucleotides including:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Reagent solution preparation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mobile phase preparation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Column Packing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fraction collection\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform oligonucleotide/intermediate analysis via LCMS\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate with cross-functional groups such as Process Development, Analytical Development, Quality Control, Quality Assurance, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a clean work space\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain safety by wearing required personal protective equipment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track and update raw material usage in D365 ERP software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as production campaign lead\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with new personnel training\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in a scientific field OR appropriate work experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Entry level to 2 years experience in a similar position\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Good verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to pay attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in a GMP setting and controlled documentation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$60,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$70,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5133490007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4630310007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5133490007,"updated_at":"2026-05-08T18:58:31-04:00","requisition_id":"857","title":"Associate Medical Director / Medical Director","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-08T18:58:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Medical Director/Medical Director will report to the head of cardiometabolic clinical development and will be instrumental in bringing important new therapies based on RNA interference to patients. This individual will work collaboratively with Arrowhead’s scientific and clinical teams to take drugs from late clinical research to NDA filings and will initially focus on siRNA programs targeting cardiac and metabolic (lipids and obesity) indications.\u0026amp;nbsp; The Associate Medical Director will take hands on responsibility for designing and managing clinical studies to evaluate the efficacy, safety, dose selection and clinical pharmacology of product candidates.\u0026amp;nbsp; Candidates with the requisite experience may be considered for a Medical Director title.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a fulltime, onsite position based from Arrowhead’s Corporate Headquarters in Pasadena, CA.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the conceptualization and design, development, execution and communication of clinical studies across a variety of therapeutic areas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a medical lead in a cross functional team that includes medical, scientific, clinical, safety, program management and regulatory staff\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively communicate protocols and other relevant information with clinical site investigators and staff\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interpret clinical trial data and communicate results clearly and accurately\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing clinical monitoring for clinical trials including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to documents, including IRB submissions, protocols, study reports, publications and regulatory submissions – including anticipated upcoming NDA/MAA submission\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide high level and complex scientific and clinical guidance to Clinical Trials Management, Biometrics, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify key opinion leaders and participate in clinical advisory board meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Make scientific presentations at advisory boards, key scientific meetings and external committee meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and evaluate medical need and clinical path for new applications of RNA interference for the treatment of disease\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and understand new developments in RNA interference in industry and academia\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support in-licensing and out-licensing activities and partner relationships\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;M.D. or MD / Ph.D. combined with research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on translational research experience within a pharmaceutical or biotechnology company or in an academic setting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated understanding of the drug development process and a strong desire to contribute to the development of meaningful therapeutics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of Good Clinical Practices, FDA regulations and guidelines and applicable regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to effectively evaluate outside expert advice\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to clearly elucidate complex scientific and medical concepts via written and oral communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working independently and effectively in a fast-paced, team-based environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong clinical/scientific/technical skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills and the ability to communicate effectively with people in diverse and different settings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses sense of urgency; identifies challenges and problems and takes the initiative to identify solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project management skills and focus on delivery of results\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Fellowship training (eg cardiology, endocrinology)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Research focused on lipids or obesity\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$260,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$310,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005299007,"name":"Clinical Development","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5149544007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4638212007,"location":{"name":"Madison, Wisconsin, United States"},"metadata":null,"id":5149544007,"updated_at":"2026-06-01T11:54:25-04:00","requisition_id":"876","title":"Associate Scientist II, Bioassays","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-28T19:40:52-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is seeking a highly motivated molecular biologist to join our growing Molecular Biology team at our Madison site. The Molecular Biology team supports R\u0026amp;amp;D projects across all sites. The ideal candidate should have 1-2 years of cloning experience with the ability to independently work on multiple constructs simultaneously.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support in vitro, ex vivo and/or in vivo studies to facilitate drug discovery and development with some independence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Propose methods and ways to optimize cloning\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasionally present research findings to project teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasionally read relevant scientific literature and propose applications to projects to troubleshoot and solve problems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a high level of productivity and quality in the lab\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform critical experiments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Primary Molecular Biology Responsibilities:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Clone plasmid constructs by various methods (Digest/ligation, IVA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform large-scale plasmid preps\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Autoclave glassware and media\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage lab inventory and assist in ordering\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project documentation\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Snapgene and Benchling experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Work with a small team of scientists, while working closely with other research groups and senior managers\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor of Science in Biology or related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in cell biology, molecular biology, immunology, pharmacology or a related field of biology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in standard cellular and molecular biology techniques (PCR, Digestion, Ligation, Transformation, DNA isolation)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in standard microbiology techniques (Bacterial cultures, Autoclaving, Preparing Media)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in standard cell culture techniques (passaging, transfection)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated innovation, creativity and resilience in problem solving\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent oral and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated team player with the ability to thrive in a fast paced, multi-disciplinary, matrixed environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;2+ years experience with methods and technologies involving plasmid cloning, AAV packaging, protein expression vectors, microbiology including bacterial cultures and autoclaving, cell culture including transfections and cell line maintenance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with Benchling and Snapgene\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$70,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$80,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005285007,"name":"Biology","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5142819007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4634838007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5142819007,"updated_at":"2026-05-20T11:11:39-04:00","requisition_id":"866","title":"Associate Scientist II, CMC Analytical Development","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-20T11:11:39-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position is in the Analytical Development (AD) Group within the CMC Manufacturing Organization.\u0026amp;nbsp; An Associate Scientist II will support method development/validation activities for new drug substances and drug product. The Associate Scientist II\u0026amp;nbsp; will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies.\u0026amp;nbsp; This position reports to either AD Management, or Senior AD staff.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Know and adhere to cGMP policies and procedures and relevant SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with team members to provide accurate analytical results in support of new and on-going projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with supervision to meet project timelines and deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform testing of samples to support batch release and stability studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform portions of analytical techniques, such as HPLC, GC, FTIR, UV/Vis, LC/MS, KF, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with the design and initiation for development of analytical methods and improvement of existing ones to support all stages of drug development process\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Handle, analyze and characterize chemicals, pharmaceuticals, and related organic molecules\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and interpret scientific data and provide the significance of such with supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the design and execution of non-routine experiments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze data/results and interpret outcome of experiments and propose appropriate follow-up for straightforward studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compile data tables of results, certificate of analysis, and develop stability reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Write analytical test methods and protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Calibrate, maintain, and troubleshoot simple and some complex analytical equipment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S in Chemistry (or related area of study)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 3 years of experience working in a chemistry laboratory setting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiar with analytical instrumentation, test methodology/validations, data acquisition systems, and cGMP policies and practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to correctly analyze data/results and interpret outcome of experiments and to propose appropriate follow-up.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works well with others and in a team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible with changing priorities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$65,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$78,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005288007,"name":"Chemistry Manufacturing \u0026 Controls","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5149564007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4638221007,"location":{"name":"San Diego, California, United States"},"metadata":null,"id":5149564007,"updated_at":"2026-05-28T19:55:37-04:00","requisition_id":"877","title":"Associate Scientist I, In Vivo Research","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-28T19:55:37-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is seeking a highly motivated biologist to join our growing CNS\u0026amp;nbsp;\u0026lt;em\u0026gt;in vivo\u0026lt;/em\u0026gt; team within the Research Department at our San Diego site. The successful candidate will be joining a team dedicated to discovering, developing and translating novel drug targets.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform in vivo studies to facilitate drug discovery and development in various diseases\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish new preclinical animal disease models\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform animal behavior studies as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate processes across departments and with outside vendors to enable efficient study execution and data generation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Read and apply relevant scientific literature to projects to troubleshoot and solve problems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present research findings to project teams and prepare technical reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a high level of productivity in the lab and perform critical experiments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS and/or MS in biology related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of extensive experience with small animal handling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent record keeping and experience in data analysis, graphing and presentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and to handle multiple projects and deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated innovation, creativity and resilience in problem solving\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent oral and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated team player with the ability to thrive in a fast paced, multi-disciplinary, matrixed environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with CNS surgeries and/or drug administration locally in CNS\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with in vivo epilepsy and/or migraine models\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Preclinical disease model development in the context of drug discovery\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$65,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$75,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005285007,"name":"Biology","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5161250007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4643927007,"location":{"name":"Madison, Wisconsin, United States"},"metadata":null,"id":5161250007,"updated_at":"2026-06-10T14:07:59-04:00","requisition_id":"892","title":"Associate Scientist I, In Vivo Research","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-10T14:07:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is seeking a highly motivated Associate Scientist to join our growing In Vivo Pharmacology team within the Biology Department at our Madison site. The successful candidate will be joining a team dedicated to discovering, developing, and translating novel drug targets. \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform in vivo studies to facilitate drug discovery and development in various diseases\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish new preclinical animal disease models\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform animal behavior studies as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate processes across departments and with outside vendors to enable efficient study execution and data generation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Read and apply relevant scientific literature to projects to troubleshoot and solve problems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present research findings to project teams and prepare technical reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a high level of productivity in the lab and perform critical experiments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor Degree in Biology or related field and some experience with small animal handling in a research setting (i.e. test article administration and tissue collection) - OR - an Associate Degree in a related area and 7 years of experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of extensive experience with small animal handling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent record keeping and experience in data analysis, graphing and presentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and to handle multiple projects and deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated innovation, creativity and resilience in problem solving\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent oral and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated team player with the ability to thrive in a fast paced, multi-disciplinary, matrixed environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Preclinical disease model development in the context of drug discovery\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experiences with animal dose administration and surgical procedures\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$55,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$68,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005285007,"name":"Biology","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5056259007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4520991007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5056259007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"607","title":" Biostatistician (Senior Associate)  ","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-02-18T17:55:32-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a stellar biostatistician (Senior Associate) to join our rapidly growing biometrics team to support clinical studies across Arrowhead’s expanding portfolio. As an internal expert in biostatistics, you will provide technical leadership and biostatistical input to closely collaborate with other functional teams at Arrowhead, including Clinical Development and Operations, Regulatory, Commercial, Program Management and others.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support statistical aspects of clinical trials including input on study design, randomization, sample size calculations, and statistical analysis plans (SAPs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft and contribute to statistical methods sections of protocols, SAPs, and clinical study reports (CSRs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform data analyses using SAS and/or R, and assist with interpretation of results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate closely with data management and statistical programming teams to ensure high-quality data and analysis outputs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in the development of summary tables, figures, and listings for regulatory submissions and publications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in reviewing and QC of statistical outputs and documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the evaluation of statistical methodologies and explore innovative analytical techniques as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to departmental process improvements, documentation, and knowledge sharing\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in Biostatistics or Statistics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with statistical software packages (e.g., SAS and/or R)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of clinical trial phases and statistical considerations in clinical research\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail, organizational skills, and ability to manage multiple tasks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn and take direction while growing into greater independence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;1+ years of relevant experience in the pharmaceutical, biotechnology, or CRO industry, is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory guidance and industry standards (e.g., ICH E9, CDISC standards such as SDTM and ADaM)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to working with CROs or cross-functional clinical trial teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of pulmonary function therapeutic area and drug development in this TA\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$130,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005292007,"name":"Biostats \u0026 Data Management","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5143764007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4635315007,"location":{"name":"Madison, Wisconsin, United States; San Diego, California, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5143764007,"updated_at":"2026-06-05T17:08:05-04:00","requisition_id":"867","title":"Business Analyst, Finance Systems","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-21T00:33:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Serving as an entry-level liaison between Finance, Accounting, Revenue, and Procurement stakeholders and cross-functional technical teams, this position supports efforts to ensure that financial systems remain scalable, operationally efficient, and compliant with internal controls and regulatory requirements. Core process areas include Procure-to-Pay (P2P), Order-to-Cash (O2C), and Financial Close and Reporting workflows.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based onsite 5 days a week from one of Arrowhead\u0026#39;s office locations.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide day-to-day functional support to Finance, Accounting, and Procurement stakeholders, ensuring timely issue resolution and continuity of critical financial operations, under the direction of the Senior Finance Solution Architect.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in identifying and documenting process automation and digital transformation opportunities in collaboration with Finance business stakeholders and senior team members.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the development of reports, dashboards, and automation solutions using the Microsoft Power Platform (Power BI, Power Apps, Power Automate) and Microsoft Fabric enterprise data\u0026amp;nbsp;lake house, guided by the Principal Data Architect.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administer identity and access governance within Dynamics 365, including user role management, license assignment, and periodic access reviews in alignment with internal controls.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain end-user training materials and system documentation to support adoption of finance-related platforms and tools.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with intake, triage, and backlog management for Finance and Procurement system/service\u0026amp;nbsp;requests, ensuring prioritization aligns with business objectives and senior team guidance.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in Agile project delivery, contributing to sprint planning, stakeholder engagement, and on-time delivery of system enhancements under the leadership of senior team members.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay current on emerging technologies and applied AI capabilities relevant to enterprise finance\u0026amp;nbsp;operations and\u0026amp;nbsp;share relevant learnings with the broader team.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Finance, Accounting, Business Administration, Information Systems, or related discipline.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;0 - 2 years of experience supporting enterprise ERP platforms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foundational experience or academic background in core Finance, Procure-to-Pay (P2P), and Order-to-Cash (O2C) business processes.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical, written, and verbal communication skills, with an eagerness to translate business requirements into well-documented specifications for senior architects and technical teams.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage competing priorities, learn quickly in a fast-paced environment, and collaborate effectively within cross-functional teams.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Exposure to regulated industry environments, including GxP or SOX compliance frameworks in Life Sciences.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to Microsoft Dynamics 365 Finance \u0026amp;amp; Operations (F\u0026amp;amp;O).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Basic to working knowledge of Microsoft Power Platform tools (Power BI, Power Apps, Power Automate)\u0026amp;nbsp;or similar tools,\u0026amp;nbsp;hands-on coursework experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with Microsoft Data Platform technologies, including Microsoft Fabric, Azure Synapse Link, and MS SQL Server.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to regulated industry environments, including GxP or SOX compliance frameworks in Life Sciences.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$60,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$68,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$68,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$75,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null},{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null},{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null},{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5124573007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4626042007,"location":{"name":"Remote"},"metadata":null,"id":5124573007,"updated_at":"2026-06-03T17:33:43-04:00","requisition_id":"849","title":"Cardiometabolic Medical Science Liaison","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-29T18:13:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced cardiometabolic Medical Science Liaison (MSL) to join an exciting opportunity within our Medical Affairs (MA) team and work in a dynamic and collaborative environment. This is a field-based position and the candidate must be located within one of the territories .\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MSLs are responsible for developing professional relationships with healthcare professionals through scientific engagement to support clinical stage and launch molecules. MSLs engage healthcare professionals through scientific exchange and provide clinical and scientific support.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Engage with cardiologists / endocrinologists / healthcare professionals / stakeholders to educate on clinical and scientific evidence to advance treatment landscape as aligned with strategic imperatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educate on RNAi technology, hypertriglyceridemia, familial chylomicronemia syndrome, and hypercholesterolemia.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize and communicate clinical and scientific insights to internal stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend and present at scientific congresses and meetings to stay up to date with the latest scientific developments and trends in cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to unsolicited inquiries consistent with MSL compliance standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company sponsored clinical trials through investigator site engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support speaker training as requested and ensure speakers are up to date with evolving disease and product data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support national, regional, and local scientific congresses including Opinion Leader (OL) engagement, session coverage, booth, and company debriefs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and analyze scientific publications, clinical trials, and competitive landscape in the cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain clinical and scientific expertise and general industry business acumen.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advance MSL value proposition, demonstrate tact and professionalism, and deliver results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act in accordance with company policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop territory specific OL and account plans including OL profiles, pre-call planning, and follow up plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate clinical and scientific information in an accurate and clear manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document MSL quantitative and qualitative accomplishments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide scientific support for Med Info inquiries, ensuring accurate and timely responses to healthcare professionals\u0026#39; queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop scientific content for medical education initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Medical Affairs as needed with special projects and initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sophisticated cross-functional relationship management is critical for success.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD, PharmD, MD, or DO degree required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of experience as an MSL\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cardiometabolic therapeutic experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Industry experience in Medical Affairs at a biotech or pharma\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level verbal and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to effectively collaborate in a dynamic environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong comprehension of cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret key scientific data and translate the findings to meet educational and research needs to affect corporate research strategic activities/decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to identify the unmet medical, educational, and research needs at a local \u0026amp;amp; regional level in the medical community.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An understanding of the health care delivery system, including the managed care arena and its impact on patient care, regional medical care and the pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of the design and execution of research studies and strategic implications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to drive results at a high level of quality as a strategic and creative thinker.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates ability to deal with ambiguity and thrive in an ever-changing environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills with demonstrated ability to manage projects and/or colleagues in successful implementation of business-critical projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong time management \u0026amp;amp; organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Pay Range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$190,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$210,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052374007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4008768007,"name":"Remote, USA","location":"Remote","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5121279007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4624493007,"location":{"name":"Remote, Outside USA"},"metadata":null,"id":5121279007,"updated_at":"2026-04-30T14:56:09-04:00","requisition_id":"844","title":"Cardiometabolic Medical Science Liaison","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-27T11:30:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;91\u0026quot; data-end=\u0026quot;433\u0026quot;\u0026gt;We are seeking an experienced cardiometabolic Medical Science Liaison (MSL) to join our Medical Affairs (MA) team in a dynamic, collaborative environment. This field-based role offers a unique opportunity to support the advancement of innovative clinical-stage and launch-ready therapies that have the potential to improve patient outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;440\u0026quot; data-end=\u0026quot;778\u0026quot;\u0026gt;In this role, you will build and maintain trusted relationships with healthcare professionals through high-quality scientific engagement. You will lead scientific exchange, deliver clinical and scientific insights, and serve as a key partner in ensuring the appropriate understanding and use of our therapies across the medical community.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Engage with cardiologists / endocrinologists / healthcare professionals / stakeholders to educate on clinical and scientific evidence to advance treatment landscape as aligned with strategic imperatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educate on RNAi technology, hypertriglyceridemia, familial chylomicronemia syndrome, and hypercholesterolemia.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize and communicate clinical and scientific insights to internal stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend and present at scientific congresses and meetings to stay up to date with the latest scientific developments and trends in cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to unsolicited inquiries consistent with MSL compliance standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company sponsored clinical trials through investigator site engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support speaker training as requested and ensure speakers are up to date with evolving disease and product data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support national, regional, and local scientific congresses including Opinion Leader (OL) engagement, session coverage, booth, and company debriefs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and analyze scientific publications, clinical trials, and competitive landscape in the cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain clinical and scientific expertise and general industry business acumen.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advance MSL value proposition, demonstrate tact and professionalism, and deliver results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act in accordance with company policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop territory specific OL and account plans including OL profiles, pre-call planning, and follow up plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate clinical and scientific information in an accurate and clear manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document MSL quantitative and qualitative accomplishments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide scientific support for Med Info inquiries, ensuring accurate and timely responses to healthcare professionals\u0026#39; queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop scientific content for medical education initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Medical Affairs as needed with special projects and initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sophisticated cross-functional relationship management is critical for success.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BPharm/MPharm, MBBS or MD, or PhD degree (or equivalent)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Five or more years of experience as an MSL\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cardiometabolic therapeutic experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level verbal and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to effectively collaborate in a dynamic environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong comprehension of cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret key scientific data and translate the findings to meet educational and research needs to affect corporate research strategic activities/decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to identify the unmet medical, educational, and research needs at a local \u0026amp;amp; regional level in the medical community.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An understanding of the health care delivery system, including the managed care arena and its impact on patient care, regional medical care and the pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of the design and execution of research studies and strategic implications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to drive results at a high level of quality as a strategic and creative thinker.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates ability to deal with ambiguity and thrive in an ever-changing environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills with demonstrated ability to manage projects and/or colleagues in successful implementation of business-critical projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong time management \u0026amp;amp; organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel (national and international) will be required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052374007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4057042007,"name":"Remote, Outside USA","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5155046007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4640891007,"location":{"name":"Remote"},"metadata":null,"id":5155046007,"updated_at":"2026-06-03T17:32:19-04:00","requisition_id":"890","title":"Cardiometabolic Medical Science Liaison (Mid-Atlantic)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-03T17:32:19-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced cardiometabolic Medical Science Liaison (MSL) to join an exciting opportunity within our Medical Affairs (MA) team and work in a dynamic and collaborative environment. This is a field-based position and the candidate must be located within one of the territories.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MSLs are responsible for developing professional relationships with healthcare professionals through scientific engagement to support clinical stage and launch molecules. MSLs engage healthcare professionals through scientific exchange and provide clinical and scientific support.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Engage with cardiologists / endocrinologists / healthcare professionals / stakeholders to educate on clinical and scientific evidence to advance treatment landscape as aligned with strategic imperatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educate on RNAi technology, hypertriglyceridemia, familial chylomicronemia syndrome, and hypercholesterolemia.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize and communicate clinical and scientific insights to internal stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend and present at scientific congresses and meetings to stay up to date with the latest scientific developments and trends in cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to unsolicited inquiries consistent with MSL compliance standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company sponsored clinical trials through investigator site engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support speaker training as requested and ensure speakers are up to date with evolving disease and product data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support national, regional, and local scientific congresses including Opinion Leader (OL) engagement, session coverage, booth, and company debriefs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and analyze scientific publications, clinical trials, and competitive landscape in the cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain clinical and scientific expertise and general industry business acumen.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advance MSL value proposition, demonstrate tact and professionalism, and deliver results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act in accordance with company policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop territory specific OL and account plans including OL profiles, pre-call planning, and follow up plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate clinical and scientific information in an accurate and clear manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document MSL quantitative and qualitative accomplishments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide scientific support for Med Info inquiries, ensuring accurate and timely responses to healthcare professionals\u0026#39; queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop scientific content for medical education initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Medical Affairs as needed with special projects and initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sophisticated cross-functional relationship management is critical for success.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD, PharmD, MD, or DO degree required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of experience as an MSL\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cardiometabolic therapeutic experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Industry experience in Medical Affairs at a biotech or pharma\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level verbal and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to effectively collaborate in a dynamic environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong comprehension of cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret key scientific data and translate the findings to meet educational and research needs to affect corporate research strategic activities/decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to identify the unmet medical, educational, and research needs at a local \u0026amp;amp; regional level in the medical community.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An understanding of the health care delivery system, including the managed care arena and its impact on patient care, regional medical care and the pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of the design and execution of research studies and strategic implications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to drive results at a high level of quality as a strategic and creative thinker.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates ability to deal with ambiguity and thrive in an ever-changing environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills with demonstrated ability to manage projects and/or colleagues in successful implementation of business-critical projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong time management \u0026amp;amp; organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Pay Range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$190,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$210,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052374007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4008768007,"name":"Remote, USA","location":"Remote","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5147112007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4636994007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5147112007,"updated_at":"2026-05-27T11:54:55-04:00","requisition_id":"873","title":"Coordinator I, Plant Operations","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-26T18:31:11-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Coordinator I, Plant Operations will play a pivotal role in ensuring the smooth execution of day-to-day operational activities. This position will support cross-functional teams, oversee project resource allocation, and assist in maintaining compliance with industry regulations. The ideal candidate thrives in a fast-paced environment and has a passion for operational excellence in the pharmaceutical industry.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain project timelines, schedule meetings, complete meeting minutes, track action items, and generate reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor, generate, and summarize departmental performance metrics to support data-driven decision-making and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in supporting complex, cross-functional projects within the plant operations team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track project plans to ensure they meet business objectives and are completed on time and within budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with manufacturing, quality, supply chain, facilities, and engineering teams to support the streamlining of workflows and resolution of operational challenges.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify inefficiencies in operational processes and recommend solutions for improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a liaison between departments to ensure clear communication of priorities and deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Submit purchase orders, review vendor invoices and approve invoices as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with the finance department to monitor departmental expenditures to ensure budget compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the coordination and execution of daily, weekly, and monthly operational tasks, ensuring alignment with department priorities and goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support functions within the document management system to ensure readiness for audits and regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Chemistry, Biology, Engineering, or other scientific related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational and time-management skills with a keen eye for detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in using D365, Smartsheet and Microsoft Office Suite.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communication skills, both written and verbal.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multitask and adapt to changing priorities in a dynamic environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;2+ years of experience in operations or coordination roles within pharmaceutical or a similar industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of GMP, FDA regulations, and pharmaceutical manufacturing processes.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$50,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$60,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5077269007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4604289007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5077269007,"updated_at":"2026-05-28T21:01:45-04:00","requisition_id":"791","title":"Corporate Counsel - Market Access \u0026 Pricing","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-12T10:55:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Corporate Counsel (Market Access and Pricing), will report to and operate under the direction of the Assistant General Counsel, supporting the provision of day-to-day strategic and business-focused legal and risk counseling to internal stakeholders primarily on the pricing, reimbursement, access, and trade and distribution of Arrowhead’s products, supporting US and global markets. \u0026amp;nbsp;You will work closely with colleagues on the legal team and across commercial, contracts, and other internal teams to lead legal strategies and support various aspects of the distribution and commercialization of Arrowhead’s products.\u0026amp;nbsp; Our relatively small legal department additionally offers the opportunity for you to develop other areas of interest.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Supporting business functions across the Company, this role requires the ability to manage multiple priorities in a dynamic, fast-paced environment, while providing proactive and collaborative legal advice to mitigate risk and ensure alignment with applicable laws and global healthcare compliance standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in office 5 days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Providing strategic counsel to Company stakeholders on issues impacting drug pricing, reimbursement, and market access, including by:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serving as an enterprise expert on federal supply schedule contracting and federal and state pricing requirements and implications, including advising on the Company’s compliance with government price laws, including price reporting requirements, the Medicaid Drug Rebate Program (including State supplemental rebate requests), Medicare Part D Manufacturer Discount Program (MDP), 340B program, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advising on the Company’s arrangements and interactions with pharmacy benefit managers (PBM), health plans, employers, governments and other payers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing legal guidance on trade and distribution strategies, patient support programs, state price reporting, government programs and pricing implications, rebate and discount arrangements, value-based agreements and payer communications\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Negotiating and drafting agreements in connection with the activities described above\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing legal guidance and oversight for activities performed by third party contractors that provide market access, government invoicing and price reporting, and distribution services on Arrowhead’s behalf.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage outside counsel as needed, particularly with respect to ex-US requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serving as a secondary legal representative on Arrowhead’s Medical Legal Regulatory (MLR) Review Committee\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp; \u0026lt;em\u0026gt;Other responsibilities may also include\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assisting in the legal team to support issues related to FDA promotional laws, the intersection between medical and marketing personnel, planning and use of real-world evidence/data, or federal healthcare program compliance strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engaging, as needed, with government or regulatory agencies to educate on the implications of specific policies or laws, represent Arrowhead’s legal perspective, and/or influence industry-wide policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Preparing and delivering training to the organization related to applicable legal areas such as contracting and risk mitigation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;3 years of experience with a substantial practice involving trade and distribution, government pricing, payer contracting, or a similar related field, at a reputable law firm or in-house at a pharmaceutical or medical device company, or a combination of both.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;J.D., licensed to practice law in the U.S. and permitted to practice law in California (including as Registered In-House Counsel)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active membership and in good standing in a state bar\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of and experience with fraud and abuse laws, particularly in the context of payer and PBM agreements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with competition, pricing, reimbursement, and access issues as they pertain to the pharmaceutical industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge and understanding of government pricing programs, including the Medicaid Drug Rebate Program, 340B, the Federal Supply Schedule, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of applicable statutory and regulatory frameworks governing the sale and marketing of pharmaceuticals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent oral and written communication skills, with an understanding of how to identify and advise on risk and strategy, presenting complex information accurately and concisely to effectuate influence appropriately (including a proven ability to communicate legal risks and mitigation strategies to senior management)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical ability, critical and strategic thinking skills, attention to detail and time management skills to appropriately manage competing priorities on aggressive timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong business acumen and an ability to provide practical, risk-based advice in a highly-regulated environment to help drive effective decision making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound conflict resolution skills and ability to work in a collaborative, global environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$200,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005295007,"name":"Legal","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5153429007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4640100007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5153429007,"updated_at":"2026-06-02T16:35:29-04:00","requisition_id":"889","title":"Director, Contracts \u0026 Pricing","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-02T16:00:45-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s Market Access team is expanding its capabilities to support current and future product launches. The Director, Contracts \u0026amp;amp; Pricing is a critical leadership role responsible for developing, optimizing, and executing pricing and contracting strategies across all stages of the Arrowhead product lifecycle. This individual will help ensure competitive positioning, maximize patient access, and enhance overall brand and enterprise value.\u0026amp;nbsp; The position reports to the Executive Director, Market Access.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in the office five days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the development and execution of pricing and contracting strategies for pre-launch and in-market brands, aligned with overarching commercial goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the creation of clear, compelling business cases to secure approval for major contracting initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuously monitor market dynamics, policy changes, and competitor pricing to inform recommendations and maintain competitive advantage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with Legal, Sales, Finance, and other functions to refine pricing and contracting strategies and ensure optimal product commercialization and profitability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Payer Team during key customer engagements and negotiations, representing pricing and contracting as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide pricing and reimbursement insights to help evaluate U.S. policy and legislative developments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Finance to support quarterly close processes, including discount forecasting, GTN analytics, and utilization by contract segment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous improvement and innovation in pricing and contracting processes, tools, and governance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with all federal, state, and company policies related to pricing, contracting, and market access activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in finance, economics, accounting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in the biotech or pharmaceutical industry, including at least 5+ years in Market Access, Contracts \u0026amp;amp; Pricing, or related functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience building, leading, and executing pricing and contracting strategies within the pharmaceutical or biotechnology industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in pricing and contracting analytics, including GTN forecasting and modeling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience developing contract proposals, including financial modeling, ROI assessments, and evaluation of GTN implications, along with demonstrated negotiation strategy capability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of pharmaceutical contract administration systems and reporting across payer, provider, government, specialty pharmacy, and distribution channels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert knowledge of pharmacy benefits; Medicare FFS and Managed Care; Medicaid; and federal purchasing programs (e.g., VA/DoD, 340B).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Subject-matter expertise in the Inflation Reduction Act (IRA), including financial risks and strategic opportunities for manufacturers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, and presentation skills, with the ability to translate complex concepts for diverse audiences\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional attention to detail, with the ability to work independently and collaboratively across cross-functional teams, external partners, and vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel as needed to engage with customers, as required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (e.g., MBA or Master’s in a related field).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Passion for science-driven storytelling and an interest in Arrowhead’s mission to advance RNAi-based therapeutics.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$230,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$250,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005300007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5143798007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4635337007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5143798007,"updated_at":"2026-05-21T01:20:03-04:00","requisition_id":"869","title":"Director, Corporate Communications","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-21T01:20:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals is seeking a seasoned and forward-thinking Director of Corporate Communications to drive corporate communications that elevate the company’s reputation and visibility while strategically supporting the launch of new products within the broader corporate narrative. Reporting directly to the SVP, Investor Relations and Corporate Communications, this individual will play a critical role in shaping Arrowhead’s corporate presence, developing and implementing communication strategies and tactics that advance our corporate image, highlight our science and innovation, and support upcoming commercial milestones.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re looking for a dynamic communicator and strategic storyteller who thrives in a fast-paced, highly regulated environment and can translate complex scientific and business narratives into clear, engaging messages that resonate with diverse audiences.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in the office five days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Strategic Planning \u0026amp;amp; Execution - \u0026lt;/strong\u0026gt;Design and deliver comprehensive communication strategies that advance Arrowhead’s corporate reputation and support key initiatives, including the launch of plozasiran and broader pipeline milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Corporate and Digital Presence -\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Lead the strategy, management, and evolution of Arrowhead’s global website and social media platforms to ensure consistent, impactful brand storytelling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Content Development -\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Craft high-quality written materials—including company narratives, executive communications, press releases, social content, op-eds, and presentations—that align with Arrowhead’s voice and objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Agency Oversight -\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Direct and collaborate with external communications partners to ensure the delivery of high-caliber, on-brand work that drives measurable impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Collaboration -\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Partner closely with Investor Relations, HR, Marketing, Medical, Legal, and other internal teams to align corporate messaging across all touchpoints.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Operational Excellence -\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Support effective budget management and resource allocation for communications programs and agency engagements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Communications, Public Relations, Journalism, Marketing, or a related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10 years of progressively responsible experience in corporate communications, public relations, or related fields—preferably within the biotechnology, pharmaceutical, or healthcare industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to develop and implement integrated communications strategies that advance corporate reputation and support business goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional writing, editing, and storytelling skills with experience crafting content for senior executives, media, and digital channels.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success managing media outreach, developing press materials, and preparing leaders for interviews and speaking engagements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of corporate digital strategy, including website management, social media, and content optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to effectively partner across departments such as Investor Relations, Marketing, Medical Affairs, and Legal to ensure alignment and compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading teams or agency partners, managing budgets, and delivering results under tight deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of regulatory and compliance considerations in healthcare communications, with sound judgment in sensitive or high-profile situations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple projects simultaneously and meet deadlines in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You may be required to travel approximately 10 -15%.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (e.g., MBA, Master’s in Communications, or related field).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing corporate branding, thought leadership, and executive visibility programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success supporting product launches or scientific communications in the life sciences sector.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in crisis or issues management, with the ability to counsel senior leaders on reputation-sensitive topics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with investor and financial communications, including message alignment between communications and IR functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of global communications practices and experience managing multi-market campaigns.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Passion for science-driven storytelling and an interest in Arrowhead’s mission to advance RNAi-based therapeutics.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$190,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$220,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005296007,"name":"Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5146360007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4636642007,"location":{"name":"Madison, Wisconsin, United States; San Diego, California, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5146360007,"updated_at":"2026-05-26T10:40:27-04:00","requisition_id":"872","title":"Director, IT Infrastructure ","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-26T10:40:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director of IT Infrastructure is a leadership role responsible for the strategy, design, implementation, and ongoing operations of the company’s enterprise IT infrastructure. This leader will oversee a geographically distributed environment spanning on-premises and public cloud platforms (Microsoft Azure and Amazon Web Services). The Director will lead a team of infrastructure staff to support business needs, drive modernization initiatives, and ensure the reliability and scalability of all infrastructure services in alignment with pharmaceutical industry standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based onsite 5 days a week from one of Arrowhead\u0026#39;s office locations.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and execute a multi-year IT infrastructure roadmap aligned with corporate growth objectives and digital transformation priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead, mentor, and develop a high-performing infrastructure team across multiple sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with the IS leadership and business stakeholders to align infrastructure investments with organizational priorities and compliance requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and manage infrastructure budgets, vendor contracts, and technology refresh cycles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and communicate infrastructure KPIs, SLAs, and operational metrics to IS leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and execute a multi-year IT infrastructure roadmap aligned with corporate growth objectives and digital transformation priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the design, deployment, and lifecycle management of virtualization infrastructure across all company locations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage a Microsoft Active Directory environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive hybrid cloud strategy and operations across Azure and AWS, optimizing workload placement, cost, and performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure high availability, disaster recovery, and business continuity capabilities for all critical infrastructure components.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee network infrastructure including LAN/WAN and SD-WAN connectivity across all company sites and cloud tenants.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee server patching and configuration management standards across the enterprise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead capacity planning and performance monitoring to ensure infrastructure scalability in support of business growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all infrastructure platforms and processes comply with regulatory requirements as applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support internal and external audits by providing documentation, evidence, and technical guidance related to infrastructure controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and test disaster recovery and incident response plans in partnership with IS and business teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead infrastructure-related projects from inception through delivery, including consolidations, cloud migrations, and site expansions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage relationships with key technology vendors and MSPs, negotiating contracts and ensuring service delivery accountability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and recommend emerging technologies that drive operational efficiency and cost reduction.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in Computer Science, Information Systems, Information Technology, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of progressive IT infrastructure experience, with at least 4 years in a senior leadership or director-level role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep hands-on expertise with virtualization platforms (VMware, Nutanix, Hyper-V).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience managing Microsoft Active Directory.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of AWS and Azure — architecture, operations, cost management, and security.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing multi-site enterprise IT environments in a regulated industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of building, leading, and developing high-performing infrastructure teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of network architecture, security principles, and ITIL-based service management frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with infrastructure compliance frameworks relevant to pharma/biotech (GxP, SOX, HIPAA).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Current or previous industry certifications such as VMware VCP/VCAP, Azure Administrator/Architect, AWS Solutions Architect, or ITIL v4.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with infrastructure-as-code tools such as Terraform, Ansible, or Bicep.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting laboratory and manufacturing IT environments (OT/IT convergence) within a pharmaceutical or life sciences setting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and the ability to translate business needs into scalable infrastructure solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills - able to present complex technical topics clearly to non-technical audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional organizational and prioritization skills in a fast-paced, regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative leadership style with a strong emphasis on team development and cross-functional partnership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data-driven decision-making and a continuous improvement mindset.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$190,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$210,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$230,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null},{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null},{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5025830007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4565405007,"location":{"name":"Madison, Wisconsin, United States; San Diego, California, United States"},"metadata":null,"id":5025830007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"641","title":"Director, Pharmacometrics \u0026 Clinical Pharmacology","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-01-15T15:50:16-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;311\u0026quot; data-end=\u0026quot;709\u0026quot;\u0026gt;Arrowhead Pharmaceuticals is seeking a Director of Pharmacometrics and Clinical Pharmacology to provide strategic and scientific leadership across the company’s clinical development programs. This senior-level role is responsible for advancing pharmacometric and clinical pharmacology strategies to support the global development and regulatory submission of Arrowhead’s leading siRNA therapeutics.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;711\u0026quot; data-end=\u0026quot;988\u0026quot;\u0026gt;The Director will play a critical role in clinical trial design, data analysis, regulatory documentation, and cross-functional decision-making, ensuring that dosing strategies and clinical pharmacology plans are scientifically rigorous and aligned with regulatory expectations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Provide leadership and subject matter expertise in pharmacometrics and clinical pharmacology across Arrowhead’s development portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Contribute to global regulatory submissions, including marketing applications for siRNA-based therapeutics.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Design and support clinical trial protocols, including dose selection and optimization strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Author and review clinical pharmacology sections of Investigational Brochures (IBs), Clinical Study Reports (CSRs), and other regulatory documents.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Conduct and oversee analysis of clinical and translational PK/PD data, including population PK/PD modeling.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Communicate analysis results, interpretation, and strategic recommendations to project teams in a timely and effective manner.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Develop clinical pharmacology plans and propose dosing strategies across development stages.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1018\u0026quot; data-end=\u0026quot;1154\u0026quot;\u0026gt;Maintain current knowledge of clinical pharmacology literature, regulatory guidance, and best practices relevant to oligonucleotide and RNAi therapeutics.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Doctoral degree (PhD, PharmD) in pharmacokinetics, pharmacology, pharmaceutical sciences, or a related discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8 years of post-degree experience in the pharmaceutical or biotechnology industry in pharmacometrics or clinical pharmacology roles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise in population PK/PD modeling, with proficiency in standard software platforms such as NONMEM.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting regulatory submissions and interacting with cross-functional development teams.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with PBPK/PD or quantitative systems pharmacology (QSP) modeling\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$200,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$225,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$220,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$245,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005298007,"name":"Clinical Pharmacology \u0026 DMPK","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null},{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5096426007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4612788007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5096426007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"827","title":"Director, Regulatory Affairs (Labeling, Advertising and Promotion)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-01T15:00:05-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director provides strategic and operational leadership for regulatory labeling and promotional activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the labeling lead, the Director will be responsible for the cross-functional development and execution of global regulatory labeling strategy for Arrowhead’s pipeline, late stage, and marketed products. This individual will manage regulatory labeling through all phases of development, during review and approval by regulators, and post-approval, ensuring that the latest requirements and standards are met.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director is also responsible for working together with legal, medical affairs and applicable stakeholders to ensure that promotional review and practices are consistent with applicable regulatory requirements, guidelines, company policies, and procedures. The Director will provide guidance, review and approve materials related to US promotional and advertising campaigns for marketed products and serve as the regulatory lead or co-lead on the US Promotional Review Committee (PRC/PCRC/MRC).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director position will report into the Executive Director of Clinical Regulatory Strategy and have line reports.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage development, review, approval, and version control of labeling documents, including Target Product Labeling, Core Labeling (e.g., Company Core Data Sheet [CCDS]), and Regional Labeling (e.g., USPI, EU SmPC), in a timely manner according to internal SOPs and external regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain expertise regarding key labeling requirements and stay current with labeling guidelines/regulations as they pertain to the development/maintenance of labeling and advise key stakeholders on the application of these labeling principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Research the content of other labels in the same therapeutic class, including competitor labeling, to help guide the team in developing labeling text, including contingency strategy development for negotiation with regulatory authorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for proofreading and departmental QC work; ensure quality of labeling deliverables (e.g., alignment of labeling text with data, regulatory requirements, consistency between labeling documents).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Liaise with cross functional members and stakeholders to obtain input pertaining to labeling including resolution of key regulatory issues and labeling changes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide operational oversight for MRC and PRC activities, generate SOPs, and conduct process improvement for advertising and promotional review\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position requires frequent interaction and strong collaboration with Commercial, Medical Affairs, and Legal, for the purpose of providing regulatory advice and guidance during promotional plan development\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for leading interactions and all submissions to FDA Office of Prescription Drug Promotion (OPDP) and Advertising and Promotion Labeling Branch (APLB), including the timely and accurate FDA 2253 submissions of US promotional materials\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences, computer science, or related science discipline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of relevant experience in pharmaceutical, biotechnology, or life sciences industry, including leadership experience in Regulatory Affairs Operations and Publishing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in electronic submission requirements (eCTD and regional variations)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of document formatting (MS Word documents, PDFs compliance, and validation tools)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience preparing and publishing high-quality electronic regulatory dossiers with major health authorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated understanding of regulatory systems from both business process and end-user perspectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to maintain highest degree of professionalism, integrity and diplomacy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with regulatory information management systems (e.g., Veeva RIM).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledgeable in emerging technologies, including AI applications in regulatory operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to serve as senior publishing SME and technical escalation point\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting global inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$230,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005297007,"name":"Regulatory","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5059076007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4595835007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5059076007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"767","title":"Director, Sales Operations","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-02-22T23:06:58-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Let’s do something amazing together! The Director of Sales Operations will play a pivotal role in the commercial success of Arrowhead’s leading investigational cardiometabolic medicine – Redemplo (siRNA targeting APOC3).\u0026amp;nbsp; This product has demonstrated compelling clinical data to date, has been approved by the FDA for Familial Chylomicronemia Syndrome (FCS) and is in late-stage development for the treatment of other grievous conditions, including Severe Hypertriglyceridemia (SHTG).\u0026amp;nbsp; Over time, the role will expand to cover additional indications and products in the Arrowhead portfolio.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In this key position, you will be leading Sales Operations for our field-based teams. Reporting directly to the Head of Commercial Operations and working closely with Head of Sales and Head of Marketing, you will play a crucial role in the execution of commercial strategy. \u0026amp;nbsp;Specifically, you will translate commercial objectives into plan-of-action and goals for the field-based teams, you will ensure proper sizing, targeting and incentive compensation.\u0026amp;nbsp; You will also help optimize systems (CRM) and logistics (fleet) support for the field.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in office 5 days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build the best team\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Help hire, train, and evaluate sales teams for high performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with training lead in developing industry-leading training; ensure effective training execution and ongoing updates.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Chart the course\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Help set national and regional sales targets in compliance with regulations and in alignment with forecasts. Align targeting and call planning based on business strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the design, implementation, and management of sales compensation plans and incentive programs; Adjust as necessary to ensure optimal performance; Help automate the targeting and incentive programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage field alignment, workload calculation, and territory mapping as needed. Adjust as necessary to ensure optimal performance. \u0026amp;nbsp;Collaborate with sales leadership to ensure optimal field resource allocation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build infrastructure and improve process:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In collaboration with IT: manage all data pertaining to sales and marketing to ensure smooth operations and reporting, including targeting, IC, KPIs, field sizing. Maintain customer master data. Optimize data sources for sales planning across field teams.\u0026amp;nbsp; Collaborate in the ongoing improvement of the CRM.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage Commercial Operations budget and vendor relationships.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create Insights\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define, develop, and regularly communicate business KPIs and metrics to various stakeholders, including executives and commercial leadership.\u0026amp;nbsp; Collaborate with commercial leadership and business analytics in defining and measuring the KPIs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in a business-rated or life sciences field. Strong understanding of the life sciences industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10 years of progressive commercial experience in biotechnology or pharmaceuticals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;and 5 years of experience in pharmaceutical data/sales operations; including roles such as brand management, data management, sales operations, analytics, forecasting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership and communication skills; effective vendor management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work collaboratively in a matrixed, team-based environment, with strong organizational and time management capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You may be required to travel for up to 20% of your time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience building commercial infrastructure for an emerging pharmaceutical company.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in cardiometabolic therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$205,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$235,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005300007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5113399007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4620759007,"location":{"name":"Madison, Wisconsin, United States; Pasadena, California, United States; San Diego, California, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5113399007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"840","title":"Director, Strategic Sourcing and Procurement","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-17T18:05:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals is seeking a Director of Strategic\u0026amp;nbsp;\u0026amp;nbsp; Sourcing \u0026amp;amp; Procurement to build and lead a best-in-class procurement function during a critical phase of commercial growth. This role will establish procurement frameworks and parameters as a strategic partner to R\u0026amp;amp;D, Commercial, and G\u0026amp;amp;A functions, driving cost efficiency, creating contract value and ensuring quality of vendor selection process while maintaining Arrowhead’s ability to move quickly in all aspects of our business.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a build-and-scale role: you will define strategy, create policies, implement processes, support business partners, lead negotiation teams, and hire lean, high-impact staff. Initial priorities will focus on establishing strategic sourcing methods and providing strong procurement support for Information Systems \u0026amp;amp; Informatics (IS\u0026amp;amp;I) and Commercial functions, two of the company’s most significant and rapidly growing spend areas.\u0026amp;nbsp;The Director of Strategic Sourcing \u0026amp;amp; Procurement will provide hands-on support and across these domains, with plans to build dedicated category management support to ensure depth of expertise and scalable coverage as the function matures.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Over time, this role has the potential to expand into an enterprise-wide sourcing and procurement leadership position, including ownership of direct spend and supply chain categories as the organization continues to scale.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in onsite with an expectation to be in the office five days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Build and Lead the Procurement Function\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design and implement Arrowhead’s procurement strategy, operating model, and policies, creating scalable procurement processes that enable continued success\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and lead solicitation processes (RFQs, ITBs, RFPs, etc.), providing operational support to ensure business requirements are appropriately captured and needs are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead complex negotiations, in close collaboration with business stakeholders, to maximize the value of contracts entered and ensure business requirements are achieved.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and lead a high-performing team across category management, procurement operations, and analytics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish procurement as a trusted partner across R\u0026amp;amp;D, Commercial, and Corporate functions. Embed procurement culture early in decision making and not just at the purchasing stage.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own sourcing and procurement strategy across key indirect spend categories: IS\u0026amp;amp;I (software and hardware) and commercial \u0026amp;amp; marketing agencies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Cost Optimization \u0026amp;amp; Value Creation\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Guide assessment and selection of vendors, managing key vendor contracts, including benchmarking, performance monitoring and risk mitigation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive vendor consolidation and preferred supplier strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and deliver measurable cost savings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Legal to develop standardized solicitation templates and vendor selection processes, working cross-functionally with the Contracting Team to ensure translation of solicitation requirements and negotiated terms to the resulting contracts.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support effective contract lifecycle management in collaboration with the Contracting Team, ensuring continuity of key services and effective negotiation of contract renewals and amendments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Finance to align on budgets and accruals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish supplier performance management and risk frameworks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop spend visibility and analytics capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead initiatives related to procurement systems, automation, and digital transformation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain deep knowledge of industry trends, supplier landscapes, and regulatory requirements to ensure compliance and innovation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of procurement/strategic sourcing experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years in leading successful negotiations for complex, high value contracts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in life sciences\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success managing indirect spend categories (IT, SaaS, marketing, professional services).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong negotiation experience with complex, high value contracts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience implementing procurement processes, policies and systems.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in a leadership role that built or scaled procurement teams/functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;MBA, technical graduate degree, or certification in sourcing or negotiations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing SaaS heavy environments and enterprise- wide vendor ecosystems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$170,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$200,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$180,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$210,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005296007,"name":"Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null},{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null},{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5116032007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4622110007,"location":{"name":"Madison, Wisconsin, United States; Pasadena, California, United States; San Diego, California, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5116032007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"843","title":"Executive Director, AI and Enterprise Data Management","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-21T15:51:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Executive Director of Artificial Intelligence and Enterprise Data Management will lead the strategy, development, and deployment of enterprise-wide data, generative AI, and agentic AI capabilities to accelerate innovation and improve operational efficiency, while ensuring regulatory compliance. This role will serve as a key enabler across the organization, transforming fragmented data into a strategic asset and driving AI adoption across R\u0026amp;amp;D, CMC, Clinical, Manufacturing, and G\u0026amp;amp;A functions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This leader will act as both a strategist and operator, educating the organization on emerging technologies, aligning cross-functional priorities, and delivering scalable AI and data solutions that create measurable business value.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based onsite 5 days a week from one of Arrowhead\u0026#39;s office locations.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Enterprise AI \u0026amp;amp; Data Strategy \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and execute a unified enterprise data and AI strategy aligned with company growth and R\u0026amp;amp;D and commercialization goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify high-impact AI and data opportunities across all functions (R\u0026amp;amp;D, Clinical, CMC, Manufacturing, G\u0026amp;amp;A and etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive executive alignment on AI and data strategy, including opportunities, risks, and investment priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the design and implementation of an enterprise data platform enabling data integration across R\u0026amp;amp;D, CMC, Clinical, and commercial domains\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish scalable data architecture to support real-time pipelines, advanced analytics, machine learning, agentic AI workflows, and AI-driven insights\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enable interoperability and data sharing across previously siloed systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;AI Governance \u0026amp;amp; Responsible AI\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and own the enterprise AI acceptable-use policy, responsible AI framework, and guardrails for LLM deployment in regulated (GxP) workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment with emerging regulatory guidance on AI/ML (FDA AI framework, NIST AI RMF, ISO 42001) and maintain audit-ready documentation for AI systems in regulated contexts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish AI model lifecycle governance including validation, performance monitoring (LLMOps), and deprecation procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Legal, Compliance, and Information Security to manage AI vendor risk and data privacy obligations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Data Governance \u0026amp;amp; Compliance \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish enterprise data governance frameworks including ownership, stewardship, data classification, quality standards, and lifecycle management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with regulatory requirements including GMP, GLP, GCP, SOX and data integrity standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Information Security to implement robust data protection, privacy, and AI governance guardrails\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;AI Enablement \u0026amp;amp; Deployment\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with IS and business function leaders to identify opportunities for data integration and AI-driven value creation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a bridge between technical and non-technical stakeholders to ensure adoption and impact\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with business and IS leaders to prioritize, design, and deploy AI solutions that improve decision-making and operational efficiency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee development and scaling of AI agents and technology across functions such as Commercial, Finance, HR, and Legal\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage strategic relationships with AI vendors and development partners, including contracting, performance oversight, and alignment to enterprise standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all AI tools and vendors comply with security, data governance, and regulatory requirements in partnership with Information Security and Legal\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Organizational Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and lead a high-performing, multidisciplinary team spanning data engineering, data science, AI/ML, and informatics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Integrate and scale the existing digital workspace/agent experimentation team into a formal enterprise function\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of innovation, collaboration, and continuous learning\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;12+ years of experience in data, analytics, AI/ML, or informatics leadership roles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Computer Science, Data Science, Engineering, Life Sciences, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience building and scaling enterprise data platforms and AI capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in life sciences, biotechnology, pharmaceutical industry, or technology industry\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success operating in regulated environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting commercial-stage organizations or scaling companies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of modern data architectures, cloud platforms, and AI/ML technologies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong business acumen with ability to translate strategy into execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading cross-functional transformation initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance innovation with risk management and compliance\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced Degree in Data Science, Engineering, Life Sciences or Business.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pharmaceutical industry experience\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$240,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$300,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$260,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$320,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null},{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null},{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null},{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5089075007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4609502007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5089075007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"815","title":"Executive Director, Medical Affairs (Dissemination \u0026 Evidence Generation)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-24T19:38:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Executive Director, Dissemination \u0026amp;amp; Evidence Generation at Arrowhead Pharmaceuticals is a senior Medical Affairs leader responsible for setting and executing the cardiometabolic strategy for scientific dissemination and medical value evidence across the portfolio. This individual leads the Publications team and the Medical Value Evidence \u0026amp;amp; Outcomes (MVEO) team and ensures that evidence generation and communication strategies are integrated, strategic, and aligned with corporate objectives.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role requires a strong, enterprise-minded leader who can unify scientific dissemination and value evidence under a cohesive strategy, elevate standards of execution, and serve as a respected partner. The Executive Director will be a core member of the Medical Affairs Leadership Team and help shape the broader function’s vision, priorities, and culture, reporting to the VP of Medical Affairs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a full-time, onsite position at Arrowhead’s Corporate Headquarters in Pasadena, CA.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Medical Affairs Scientific Dissemination\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and lead the overarching strategy for scientific dissemination and medical value evidence across all assets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment between evidence generation plans, publication strategy, and value demonstration priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs asset leads to integrate dissemination and evidence plans into overall product strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipate evolving external evidence expectations (clinical, payer, guideline, and policy) and adapt strategy accordingly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish clear governance, prioritization frameworks, and performance metrics across teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure high-quality, timely, and scientifically rigorous dissemination of clinical and real-world data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Promote a culture of scientific rigor, accountability, and cross-functional partnership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Medical Value Evidence \u0026amp;amp; Outcomes Leadership\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee the MVEO strategy, including health economics, real-world evidence, outcomes research, and value demonstration initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure evidence generation plans support payer engagement, reimbursement discussions, and policy positioning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Market Access to align value evidence with access strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Guide development of economic models, RWE studies, and outcomes data that strengthen product differentiation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Doctorate degree in life sciences, healthcare, or related field required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;15+ years experience in Medical Affairs or related functions within the pharmaceutical or biotech industry with a strong understanding of Medical Affairs and compliance requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant experience leading publications and/or health economics and outcomes research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success building and leading high-performing medical teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting both pipeline and commercial-stage assets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of payer evidence requirements and value communication.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational, project management, and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work effectively across functions and with external stakeholders in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage multiple projects simultaneously with strong attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced training in lipidology, cardiometabolic disease, or rare/metabolic disorders\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$280,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$320,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052374007,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5115754007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4622008007,"location":{"name":"Pasadena, California, United States; San Diego, California, United States"},"metadata":null,"id":5115754007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"842","title":"Executive Director, Regulatory Affairs","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-21T12:11:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position will report into Group Vice President, Regulatory Affairs. Executive Director, Regulatory Affairs, will be the leader of the Clinical Regulatory sub-team and will have responsibility for Clinical Regulatory submissions in the US and ex-US across the entire Arrowhead pipeline, with a focus on the EU.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Executive Director, Regulatory Affairs will provide global oversight; direction and leadership for all clinical regulatory activities related to their assigned products as well as any assigned functional support activities. The incumbent will actively develop, participate in, and manage the coordination, creation, and review of clinical regulatory strategies and all associated documents for regulatory submissions. The Executive Director, Regulatory Affairs, will ensure compliance of all associated activities, documentation quality and reporting obligations with relevant global regulatory requirements, laws and regulations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role requires onsite presence 5 days a week either in Pasadena, CA or San Diego, CA, with a preference for Pasadena, CA.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In partnership with the Group Vice President, Regulatory Affairs, provide clinical regulatory expertise and leadership to ensure the Company builds credible and trustworthy relationships with health authorities based upon the submission of scientifically meritorious data and in conformance with quality standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interacts with FDA and other international regulatory agencies as needed, on a proactive, independent, and frequent Appropriately communicates company views to agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supervise, manage, and collaborate with external service vendors, contractors and consultants as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain, generate information and documents to be submitted to regulatory authorities; prepare effective planning timelines, and liaise with team contributors for the preparation of required regulatory documents and submissions. Provide regulatory subject matter expertise during the review of documentation, protocols and reports received. Prepare additional written materials as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and interpret regulatory rules as they relate to Company products and procedures, clinical studies, testing or record-keeping and ensure they are communicated through Company policies and procedures. Recommend and implement compliance strategies for existing and proposed products and activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Take a leadership role in the development of regulatory functional infrastructure and business operations e.g. electronic documentation management systems/archiving, electronic publishing systems, documentation template development; serve as primary owner for Regulatory Affairs Standard Operating Procedures (SOPs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as backup to the Vice President, Regulatory Affairs on assigned core teams as needed; assist in submission risk assessment process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Handle various project budgets, as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasional domestic and international travel.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor of Science degree in a science-related field (with an advanced scientific degree preferred).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of relevant experience in a regulated drug environment is required. The ideal candidate will also have management experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of regulations and guidelines governing all phases (pre-IND through post-approval) of drug development and working knowledge of US and ex-US regulations and practices pertaining to the development, manufacture, testing and distribution of pharmaceutical\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of clinical regulatory requirements for clinical trials and marketing applications particularly for key countries ex-US such as EU, UK, Canada, Australia and Asia.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of regional/country-specific clinical regulatory requirements for launch requirements and post-approval life cycle management particularly for key countries ex-US such as EU, UK, Canada, Australia and Asia.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A demonstrated track record of successful regulatory filings e.g. IND/CTAs, NDA/BLA/MAAs is essential, with the ideal candidate having done several INDs and at least one registrational filing. Experience with bringing regulatory projects to commercialization is of value.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrable experience in successfully developing and managing regulatory submissions, review and preparation of scientific/technical/clinical responses to agency questions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good understanding of pharmaceutical development, clinical research and the regulatory environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience in leading a team to prepare for major regulatory agency interactions, such as FDA pre-NDA, EOP2 meetings, advisory committee meetings, and/or EU oral explanations/scientific advice.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with the electronic submission process (e.g., Veeva RIM System or equivalent); highly proficient in the functionality of MS Word, Adobe Acrobat, and PowerPoint.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$280,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$320,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005297007,"name":"Regulatory","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null},{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5123147007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4625305007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5123147007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"846","title":"GMP Investigation Lead, Quality Control","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-28T15:50:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position resides within the Quality Control function under the Quality Organization. The GMP Lead Investigator is responsible for leading, authoring, and managing deviations; OOS/OOT/Atypical laboratory investigations; and associated change control records arising from analytical testing activities. These activities include testing of environmental monitoring samples, pharmaceutical raw materials, in‑process manufacturing samples, finished drug substances and drug products, and stability samples for new drug substances and drug products within a GMP environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The incumbent will embody a GMP‑compliant quality mindset, driving excellence, continuous improvement, and ethical practices to ensure regulatory compliance and sustain the highest standards of quality. The GMP Lead Investigator serves as the primary Quality Control representative, overseeing and coordinating all investigation‑related activities conducted by the Quality Control team.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as Lead investigator and ensure the timely completion of high quality, robust GMP investigations with clearly defined and scientifically sound root cause determination\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, justify, and oversee the implementation of effective Corrective and Preventative Actions, (CAPAs) to prevent recurrence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct structured, science-based root cause analysis (RCA) using approved methodologies (5-Whys, Ishikawa, Fault Tree, etc)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Escalate events to management when they represent potential significant quality risks or may impact investigations closure timelines or product release\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support regulatory inspections and internal/external audits by maintaining inspection readiness and serving as a subject matter expert (SME) as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to site Quality Operations compliance activities in alignment with Arrowhead standards, procedures and cGMP requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross functionally with site personnel to provide guidance and drive resolution of end-to-end manufacturing and quality issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure accurate, complete, timely documentation and review of Quality Control investigations, CAPAs, Change Controls and complainants.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate historical data, trends and prior investigations for recurrence or systemic issues and opportunities for proactive improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the maintenance and improvement of investigation compliance metrics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in and contribute to continuous improvement initiatives related to the investigation and CAP processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while also collaborating effectively with cross – functional partners, including Manufacturing, Quality Assurance, Supply Chain and Project managers, external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform detailed review of batch records, stability reports, Raw material, Environmental monitoring reports, equipment logs, in-process testing, data review and other duties assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A minimum B.S. in Chemistry (or related field) with 5+ years’ work experience is required. Preferably candidate with working experience in Pharmaceutical and /or oligonucleotide manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of cGMP and GDP, iCH and FDA/EU guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Great attention to detail and ability to follow procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, pH, Osmo and/or Raman etc.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills with the ability to simplify and clearly communicate complex quality and technical concepts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, and presentation skills, including the ability to clearly articulate investigation outcomes, risk assessments, and decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to interpret quality issues and determine scientifically sound, compliant resolutions that minimize risk and withstand regulatory scrutiny.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong ability to collaborate effectively with stakeholders, customers, and peers to drive timely resolution of quality issues across the product lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven decision‑making capability, with the ability to think critically and creatively while maintaining compliance, quality standards, and GMP expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to assess the criticality of quality issues and clearly communicate complex risks, trends, and investigation outcomes to management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated understanding and application of \u0026lt;strong\u0026gt;ICH Q10 Pharmaceutical Quality System principles\u0026lt;/strong\u0026gt;, including risk management, CAPA effectiveness, knowledge management, and continuous improvement across the product lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capability to support and maintain a state of inspection readiness through accurate, complete, and traceable documentation aligned with cGMP and data integrity expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Office Suite and QMS systems such as Veeva and experience with LIMS.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$90,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$105,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5079097007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4605065007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5079097007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"802","title":"Group Manager, Product Development Operations","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-16T11:58:46-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Group Manager, PDO is a member of a team charged with ownership of end-to-end alignment of Arrowhead products from preclinical through commercial phases. This role is accountable for assigned projects and provides leadership to cross-functional CMC teams from drug substance process development through delivery of clinical kits. This role oversees both internal and external CMC activities to ensure alignment with program timelines, quality standards, and regulatory requirements. The position will have direct reports and is responsible for mentoring, performance management, and team development. In addition, this individual is partner-facing, serving as a key point of contact for stakeholders and external partners. The role will manage external relationships, including partnerships, and act as the primary contact for contract manufacturing organizations (CMOs) and contract research organizations (CROs) supporting development, analysis, manufacturing, packaging, and labeling activities for Arrowhead drug development programs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as primary point of contact for projects, facilitating communication between internal and external team members for CMC development, analytical, manufacturing, packaging, and labeling activities with minimal support of direct management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a clear understanding of project status and tailor communications appropriately for Arrowhead leadership, relevant stakeholders, and partner companies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage budget, timeline, quality and deliverables for each project and vendor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Escalate risks, drive scenario planning, and present recommendations to leadership teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and expand upon current project tracking tools (ex. Smartsheet, Excel, Power BI)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze project metrics and prepare recommendations for leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interface with cross-functional project team (Chemistry, Engineering, Analytical, Quality) on partner development and manufacturing activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track, manage, and negotiate new proposals and draft RFPs with support from technical SME’s and Legal\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Steer alignment among technical SME’s, Sourcing \u0026amp;amp; Supplier Management, Legal, and Finance on contracts, supply agreements, confidentiality agreements, and purchase orders for new and existing vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track vendor invoices and collaborate with Finance to process payments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, collect, and maintain performance metrics for internal and external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead project meetings, vendor/partner visits, and conference calls\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate internal discussions to obtain team consensus and decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive business review meetings with vendors with support from Sourcing \u0026amp;amp; Supplier Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support vendor management responsibilities and activities, as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in developing and review CMC outsourcing budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coach and mentor direct reports in the creation of personal goals, development, and performance improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate, maintain, and approve training materials and support onboarding of new team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Alliance Management on partnership goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in a scientific field such as Chemistry, Chemical Engineering, Biochemistry, Biotechnology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Eight years of increasing responsibility in a pharmaceutical company, contract manufacturing organization or contract research organization including direct report experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum five years in a project management role with experience managing clients, partners, and/or vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of applicable GLP, GMP, and regulatory guidance for pharmaceutical manufacturing and testing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong MS Office skills (Outlook, Excel, PowerPoint, and Word)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work with diverse professionals in a matrix environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated team player willing to contribute to a growing biotech organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A detail oriented, organized, self-starter who endeavors to anticipate problems and seeks opportunities to grow the role and responsibilities at Arrowhead\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Master\u0026#39;s degree in Chemistry, Chemical Engineering, Biochemistry or related science field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;GLP or GMP Laboratory or Manufacturing experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with late-stage CMC drug development and commercialization activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project Management Certification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;ERP system experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$125,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$135,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5129012007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4628052007,"location":{"name":"Madison, Wisconsin, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5129012007,"updated_at":"2026-05-05T10:55:34-04:00","requisition_id":"851","title":"GxP Laboratory Systems Administrator","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-05T10:55:34-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The GxP Laboratory Systems Administrator position is responsible for supporting the development and delivery of various laboratory systems including daily system administration of GxP systems across multiple departments including, Manufacturing, CMC, QC, BioAnalytical and DMPK, Clinical Pharmacology ad BioMarkers. The GxP Laboratory Systems Administrator will be responsible for defining standard business processes, configuring/testing/validating the software solutions, deploying the solutions across multiple Arrowhead Pharmaceuticals sites, and then supporting those software solutions. The position works closely with the business, consulting partners, and internal IS\u0026amp;amp;I teams. The GxP Laboratory Systems Administrator will serve as an expert resource, bringing forth opportunities and other complementary solutions to help support the growth of Arrowhead Pharmaceuticals and influence decisions regarding business process changes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Business\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support and system administration for identified applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform investigation and resolution efforts for technical and business process issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate technical issues and resolutions with users and department managers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Escalate issues to application vendors as necessary\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot and collaborate with end users and departmental managers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a high level of functional subject matter knowledge for the assigned applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Regulatory\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform periodic application review and management of user access\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent the application documentation in client and regulatory audits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to audit finding responses\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to computer system validation and computer software assurance projects, including application change control as required by GxP, Arrowhead Pharmaceuticals policies and SDLC\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft CSV/CSA documentation for example, validation plans, design specifications, traceability matrices, functional user and user requirements specifications, test scripts, deviations, and summary reports\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Information Systems and Informatics\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish open communication between the business and Information Systems and Informatics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Triage escalation of technical issues to Information Systems and Informatics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform updates to the global systems inventory for applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate release of new versions of applications into respective environments including Development, Testing and Production environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop business scenarios to test applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verify installation and operation of applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document analysis and/or testing related to infrastructure changes. (e.g., operating system patches, significant network changes)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in computer science or life sciences, other related field, or equivalent experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;4+ years experience related to the administration, operation, and maintenance of Laboratory Information Management Systems (LIMS) Chromatography Data Systems, Spectrophotometry Systems, and ancillary/supporting laboratory systems in a GxP environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced knowledge of computer programs (e.g., MS Word, MS Excel, computerized data acquisition systems)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multi-task and participate in multiple projects and department initiatives concurrently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to produce high quality results while working under the pressure of strict deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function effectively independently, as necessary, and work with others to achieve team goals\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience validating and supporting Agilent laboratory systems (Openlab, Chemstation, Cary UV systems)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent experience with pharmaceutical/CRO industry regulations, standards, and guidelines (GxP, CSV/CSA validation, 21 CFR Part 11, EU Annex 11, SDLC)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with regulated environment asset management applications and environment monitor applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Computer System Validation, 21 CFR Part 11, Annex 11, and GxP\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pharmaceutical or CRO experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project Management certification\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$90,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$115,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5139011007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4633059007,"location":{"name":"Madison, Wisconsin, United States"},"metadata":null,"id":5139011007,"updated_at":"2026-05-15T13:16:13-04:00","requisition_id":"863","title":"Helpdesk Technician","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-15T13:16:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals is seeking a Help Desk Technician to join the Information Technology department at our Madison, WI location. The successful candidate will be the primary point of contact for employees seeking help desk support and will focus on providing Tier I/II tech support of a Windows based network as well as stellar customer service.\u0026amp;nbsp; They will be joining a team of highly motivated and experienced IT professionals and will contribute to the success of Arrowhead programs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Frontline Help Desk support for all on-site and remote users, fielding tickets via Fresh Service and remote access tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintaining PC life cycle – imaging, deploying, migrating, retiring PCs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain IT equipment inventory and software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to employees’ inquiries regarding Windows 11, Office 365, and mobile devices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot network connectivity issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Upholding acceptable usage policies as outlined by the company handbook\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Upholding IT security best practices outlined by the IT department\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist IT management with physical networking tasks on occasion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and troubleshoot video conferencing technologies on PCs and in conference room environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Light Active Directory administration\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;2+ years of professional IT experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Windows 11 in an Active Directory Domain setting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in enterprise computer image deployment tools such as Smart Deploy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Office 365 desktop applications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency using remote support tools such as Beyond Trust\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent customer service skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Intune\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in video conference platform Team. Zoom, Webex\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Computer Science or a related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A+ certification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with ticketing systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with cloud MDM platforms\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$55,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$67,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5163400007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4644967007,"location":{"name":"Madison, Wisconsin, United States"},"metadata":null,"id":5163400007,"updated_at":"2026-06-12T11:36:18-04:00","requisition_id":"894","title":"Information Security Analyst II","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-12T11:36:18-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Information Security Systems Analyst is responsible for the day-to-day administration, operation, and continuous improvement of the organization\u0026#39;s Microsoft Purview platform, serving as the primary subject matter expert for data governance, data loss prevention (DLP), and information protection. This role operates at the intersection of information security, data governance, and regulatory compliance, ensuring that sensitive data - including intellectual property, clinical trial data, and personally identifiable information - is properly classified, protected, and governed in accordance with applicable regulations and internal policies. In addition to Purview-focused responsibilities, this analyst contributes to broader information security operations including troubleshooting endpoints, working in Microsoft 365, and Intune.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;The analyst will serve as the hands-on operational owner of Microsoft Purview, managing the platform on a daily basis across its core functional areas:\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Information Protection \u0026amp;amp; Data Classification - Administer and maintain Microsoft Purview sensitivity labels, label policies, and auto-labeling configurations. Develop and refine classification taxonomies appropriate to pharmaceutical data types, including research data, regulatory submissions, and patient data. Review and tune auto-classification rules to minimize false positives and ensure accurate labeling across Microsoft 365 and connected data sources.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Loss Prevention - Build, maintain, and continuously tune DLP policies across Exchange, SharePoint, OneDrive, Teams, and endpoints. Investigate DLP policy matches and alerts, differentiate true policy violations from false positives, and work with business stakeholders to refine rules without disrupting legitimate business workflows. Document DLP incidents and escalate confirmed violations per the incident response process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;eDiscovery \u0026amp;amp; Content Search - Support legal hold requests and eDiscovery collections. Work with Legal and HR to scope, execute, and export content searches accurately and in accordance with chain-of-custody requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Insider Risk Management - Administer Purview Insider Risk Management policies, review alerts, and coordinate with HR, Legal, and Security leadership on confirmed or suspected insider risk cases. Maintain strict confidentiality in handling all insider risk data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Audit \u0026amp;amp; Reporting - Generate and interpret Purview audit logs, compliance reports, and dashboard analytics. Provide regular reporting to management on DLP incidents, label adoption rates, policy effectiveness, and compliance posture. Identify trends and recommend adjustments to policies and configurations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Platform Administration \u0026amp;amp; Health Monitoring - Monitor the health and performance of the Purview platform, apply configuration changes and updates in alignment with change management processes, and stay current on Microsoft feature releases relevant to Purview. Manage connector integrations with third-party data sources as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain clear documentation (runbooks, diagrams, standards, exceptions) and contribute to a knowledge base.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Triage security alerts and escalate as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in Information Security, Information Technology, Computer Science, or a related field, or equivalent practical experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in Information Security, IT compliance, or data governance role\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated hands-on experience administering Microsoft Purview or its predecessor Microsoft 365 Compliance Center, including at least two of the following areas: sensitivity labels, DLP, retention policies, eDiscovery, or Insider Risk Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working within or supporting a regulated industry environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills with the ability to investigate alerts, interpret audit logs, and distinguish signal from noise\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective written and verbal communication skills, with the ability to explain technical concepts to non-technical stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Microsoft certifications relevant to security and compliance, such as SC-401\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Microsoft Defender for Cloud Apps (MCAS) and its integration with Purview\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in the pharmaceutical, biotech, or life sciences sector\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting eDiscovery or legal hold workflows in collaboration with Legal teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to SIEM tools, endpoint detection and response (EDR) platforms, or identity and access management systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable working across functional teams including Legal, Compliance, HR, and IT, and possesses the judgment to handle sensitive data and insider risk information with appropriate discretion.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$85,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$100,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5152086007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4639471007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5152086007,"updated_at":"2026-06-01T16:56:04-04:00","requisition_id":"883","title":"Lab Assistant, Manufacturing","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-01T16:56:04-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Assistant I, Manufacturing will perform basic laboratory duties involved with maintaining the cleanliness of the company’s chemical laboratories, equipment and maintaining stock levels of inventory.\u0026amp;nbsp; In addition, they will assist production chemists with routine production activities i.e., non-GMP and GMP manufacturing of oligonucleotides.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain glassware for the laboratory;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain cleanliness and orderliness of work areas;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain stocks of laboratory supplies and material and maintains appropriate records;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow safety procedures for chemical handling, as appropriate;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow batch records, SOPS, and work instructions to detail;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document all operations in batch records and notebooks;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comply with GMP protocols;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with and support operation of large scale oligonucleotide manufacturing equipment (i.e. oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to pay attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience in a laboratory setting\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Some college or concurrent college course attendance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$40,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$45,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5151979007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4639424007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5151979007,"updated_at":"2026-06-01T16:57:22-04:00","requisition_id":"881","title":"Lab Assistant, Manufacturing (2nd shift)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-01T16:01:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Assistant I, Manufacturing will perform basic laboratory duties involved with maintaining the cleanliness of the company’s chemical laboratories, equipment and maintaining stock levels of inventory.\u0026amp;nbsp; In addition, they will assist production chemists with routine production activities i.e., non-GMP and GMP manufacturing of oligonucleotides.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;2\u0026lt;sup\u0026gt;nd\u0026lt;/sup\u0026gt; shift work hours are Monday - Thursday 1pm – 11:30pm and eligible for a 10% shift differential.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain glassware for the laboratory;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain cleanliness and orderliness of work areas;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain stocks of laboratory supplies and material and maintains appropriate records;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow safety procedures for chemical handling, as appropriate;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow batch records, SOPS, and work instructions to detail;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document all operations in batch records and notebooks;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comply with GMP protocols;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with and support operation of large scale oligonucleotide manufacturing equipment (i.e. oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to pay attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience in a laboratory setting\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Some college or concurrent college course attendance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$40,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$45,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5163710007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4645116007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5163710007,"updated_at":"2026-06-12T14:52:20-04:00","requisition_id":"895","title":"Lead, Technical Transfer","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-12T14:52:20-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position will be primarily responsible for leading technical transfer activities to support manufacturing readiness. This includes writing and developing GMP batch records, methods, and other necessary documentation to ensure effective process transfer between process development and manufacturing groups. They will assist with writing and updating SOPs and technical documents pertaining to GMP operations. The position is also responsible for coordinating process transfer activities for new and existing programs across cross-functional teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work between process development and manufacturing scientists to create and maintain production batch records and process documentation for new and existing programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate cross-functional coordination and input to document new methods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage project timelines and provide project milestone updates to internal team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and implement best practices and process improvements to technical transfer activities and documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead deviation investigations and implement appropriate corrective action as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the compilation of master data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Write SOPs pertaining to GMP production.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform reviews of executed batch records\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with different departments to achieve project readiness goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasionally assist with laboratory work as needed\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3 years working in a GMP setting with a minimum of 1 year of experience in a technical writer or technical transfer position\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient experience working with controlled documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with internal CAPA investigations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient project management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to collaborate with and coordinate cross-functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with Microsoft Suite applications (Word, Excel)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multi-task and manage responsibilities within ongoing projects\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5+ year\u0026#39;s GMP experience and 3+ years tech transfer experience.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$84,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$100,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5150426007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4597349007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5150426007,"updated_at":"2026-05-29T15:14:16-04:00","requisition_id":"769","title":"Manager, Accounting (Revenue)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-29T15:14:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is seeking a Revenue Accounting Manager to join its Finance \u0026amp;amp; Accounting team at its Pasadena, CA headquarters.\u0026amp;nbsp; Reporting to the Senior Accounting Manager, \u0026amp;amp; working closely with the Controller, the Revenue Accounting Manager will manage all aspects of partnership/collaboration accounting and commercial revenue.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a newly created, high‑impact role designed to build and scale best‑in‑class revenue recognition processes in the life sciences industry, where revenue models are complex and highly specialized. The role carries full ownership of the company’s revenue framework and serves as the subject‑matter expert for ASC 606 revenue accounting. Success in this position requires a strong mix of technical accounting expertise, leadership, and cross‑functional collaboration to ensure accurate financial reporting, operational efficiency, and SOX compliance. The ideal candidate is detail‑driven, highly responsive, tech‑savvy, and adaptable in a fast‑moving environment, with 5+ years of progressive experience in finance or accounting, with a significant focus on revenue recognition (ASC 606), preferably within biotech or pharmaceutical companies.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California with an expectation to be in office 5 days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop a deep understanding of partnership and customer contracts and serve as the subject‑matter expert on revenue accounting under ASC 606 and U.S. GAAP. Review and assess complex contracts, including partnership arrangements, to determine appropriate revenue recognition treatment and disclosure requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain revenue accounting policies and procedures in accordance with regulatory standards and SOX control requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with FP\u0026amp;amp;A to lead cross‑functional efforts to ensure accurate tracking of actual labor hours, facilitate updates to budgeted resource assumptions. Ensure inputs to input‑method revenue recognition are well‑supported, accurate, and audit‑ready.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform order-to-cash month‑end and quarter-end close activities, including the preparation and posting of journal entries, completion of balance sheet reconciliations and flux analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with gross-to-net revenue accounting, including reviewing support provided by the 3\u0026lt;sup\u0026gt;rd\u0026lt;/sup\u0026gt; party and month-end close activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the preparation of revenue‑related disclosures for the Company’s Forms 10‑Q and 10‑\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and maintain SOX‑compliant controls for the revenue and accounts receivable cycles, ensuring proper execution and documentation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Accounting, Finance, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of financial accounting experience, with a significant focus on revenue recognition (ASC 606).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In‑depth knowledge of U.S. GAAP and SOX compliance requirements as they apply to revenue recognition, receivables, contract assets and deferred revenue\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage and execute complex monthly and quarterly close processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to communicate complex accounting guidance clearly and effectively to non‑finance and cross‑functional partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong capability to lead change initiatives and successfully manage complex, multi‑phase projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills, with a focus on accuracy, detail orientation and the ability to produce in tight timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, oral and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possess the highest level of integrity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to adapt to a rapidly changing environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent team player\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated with an insatiable desire to learn \u0026amp;amp; be challenged\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability for occasional travel between Arrowhead’s locations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience in a technical accounting role within the life sciences, biotech, or pharmaceutical industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Big 4 accounting firm experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Public company experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$120,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005296007,"name":"Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5080227007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4605567007,"location":{"name":"Pasadena, California, United States; San Diego, California, United States"},"metadata":null,"id":5080227007,"updated_at":"2026-05-07T18:59:03-04:00","requisition_id":"807","title":"Manager, Clinical Programming","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-16T10:35:46-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a manager for clinical programming to join our growing biometrics team to support clinical studies across Arrowhead’s expanding portfolio. This is an exciting opportunity for a candidate trained in SAS programming and data analysis is who has some prior experience working as a clinical or statistical programmer, preferably within a CRO or a similar group. Prior management experience is not needed. They will initially contribute their expertise in the area of data management/clinical or statistical programming, with a goal to develop as a lead within clinical programming.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop, and execute edit checks and patient profile software or programs for clinical trials;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute data listing programs used by data managers, safety surveillance, medical or clinical operations personnel;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with data management to ensure appropriate data collection and reporting. Participate in study team meeting and support data management activities;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Program and deliver results on time for ad-hoc data programming requests;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and help implement statistical computing environment, specifically SAS server setup and work practices;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support statistical programming, from raw data to ADaM, of efficacy and safety evaluation;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interface with CRO and perform quality audits on CRO outputs. Review outputs provided by CROs for accuracy and consistency with the programming specs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in efforts to identify, develop, and implement departmental standards, applications, processes and training; and\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop or support standard operation procedure preparation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences or technical field;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 5 years’ experience of SAS programming for clinical trials;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;s\u0026gt; \u0026lt;/s\u0026gt;Working knowledge of SAS, including complex data manipulation, data presentation and output deliver systems;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience implementing edit checks and patient profiles on active clinical trials; and\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with CDISC standards, derivation of SDTM and ADaM specifications;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data management experience;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in R; and\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CRO experience.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$120,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$140,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005292007,"name":"Biostats \u0026 Data Management","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5153072007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4639923007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5153072007,"updated_at":"2026-06-02T13:18:24-04:00","requisition_id":"887","title":"Manager, Commercial Field Sales Operations","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-02T13:18:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Let’s do something amazing together! The Manager of Sales Operations will play an important role in the commercial success of Arrowhead’s leading investigational cardiometabolic medicine – Redemplo (siRNA targeting APOC3).\u0026amp;nbsp; This product has demonstrated compelling clinical data to date, has been approved by the FDA for Familial Chylomicronemia Syndrome (FCS) and is in late-stage development for the treatment of other grievous conditions, including Severe Hypertriglyceridemia (SHTG).\u0026amp;nbsp; Over time, the role will expand to cover additional indications and products in the Arrowhead portfolio.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In this key position, you will be supporting Sales Operations for our field-based teams. Reporting to the Director of Commercial Operations and working closely with Sales and Marketing leadership, you will play an important role in the execution of commercial strategy.\u0026amp;nbsp; Specifically, you will help translate commercial objectives into plan-of-action and goals for the field-based teams, you will support proper sizing, targeting and incentive compensation.\u0026amp;nbsp; You will also help optimize systems (CRM) and manage logistics including fleet administration and support for the field.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in office 5 days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Field Excellence\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Help set national and regional sales targets in compliance with regulations and in alignment with forecasts. Help align targeting and call planning based on business strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help support the implementation and management of sales compensation plans and incentive programs; adjust as necessary to ensure optimal performance; help automate the targeting and incentive programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help manage field alignment, workload calculation, and territory mapping as needed. Adjust as necessary to ensure optimal performance.\u0026amp;nbsp; Collaborate with sales leadership to ensure optimal field resource allocation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build infrastructure and improve process\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In collaboration with IT - support management of all data pertaining to sales and marketing to ensure smooth operations and reporting, including targeting, IC, KPIs, and field sizing. Maintain customer master data. Optimize data sources for sales planning across field teams. Collaborate in the ongoing improvement of the CRM.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Commercial Operations budget tracking and assist with vendor relationships and day-to-day vendor coordination.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the field fleet program: coordinate vehicle assignments, track lease schedules and renewals, liaise with fleet vendors, ensure compliance with company fleet policy, and serve as the primary point of contact for field team fleet-related needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Create insights\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the definition, development, and regular communication of business KPIs and metrics to various stakeholders.\u0026amp;nbsp; Collaborate with commercial leadership and business analytics in tracking and reporting on KPIs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in a business-rated or life sciences field. Strong understanding of the life sciences industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of progressive commercial experience in biotechnology or pharmaceuticals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of experience in pharmaceutical data/sales operations; including roles such as brand management, data management, sales operations, analytics, forecasting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership and communication skills; effective vendor management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work collaboratively in a matrixed, team-based environment, with strong organizational and time management capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You may be required to travel for up to 20% of your time.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in the cardiometabolic disease space\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$120,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005300007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5152831007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4639825007,"location":{"name":"Pasadena, California, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5152831007,"updated_at":"2026-06-12T13:19:33-04:00","requisition_id":"886","title":"Manager, Computer Systems Assurance and Validation","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-02T11:26:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Manager, Computer Systems Assurance and Validation\u0026amp;nbsp;is a subject matter expert (SME) and project owner responsible for leading and executing computer system validation and assurance activities across the organization. The role drives a risk-based approach to validation through CSA principles and frameworks such as GAMP 5 to ensure GxP systems meet intended use while driving efficiency and compliance with applicable regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11). Acting as a key cross-functional contributor, this individual partners with Quality, IS, Manufacturing, Regulatory, Clinical, and other stakeholders to influence compliance strategy, lead validation initiatives, and actively contribute to the maturation of the company’s quality system and validation frameworks. The Manager serves in both an execution and oversight capacity depending on project scope, including signatory responsibilities on validation deliverables, and serves as a key technical voice in shaping how the organization approaches validation in a regulated GxP environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based onsite 5x a week in Pasadena, CA or Verona, WI.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Compliance Strategy \u0026amp;amp; SME Leadership\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Quality Assurance and IS leaders to support the development and implementation of risk-based CSA/CSV strategies and frameworks (CSA, GAMP 5) ensuring alignment with global regulatory requirements and industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive the adoption of CSA principles for validation projects, facilitating the shift from traditional CSV approaches toward risk-based methodologies that reduce unnecessary documentation while maintaining compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as subject matter expert (SME) on validation and compliance topics, advising internal stakeholders on best practices for software validation and assurance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain awareness of evolving regulatory expectations and support updates to company policies and procedures accordingly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Quality and cross-functional teams to develop, refine, and mature validation processes, quality systems, and frameworks, ensuring they are scalable, audit-ready, and aligned with current and emerging regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Validation \u0026amp;amp; Assurance Activities\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with System Owners to own and execute the full validation lifecycle for GxP systems, including planning, risk assessment, testing, reporting, and periodic review, applying a risk-based approach throughout.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and/or oversee validation activities depending on project scope and complexity, including serving as a signatory on validation deliverables where appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author validation deliverables (e.g., system requirements, validation plans, URS, test scripts, traceability matrices, validation reports) in accordance with regulatory expectations and internal standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply risk-based testing strategies to optimize validation efforts and focus resources on areas of greatest compliance impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead ongoing system assurance activities including periodic reviews, change management, and system decommissioning.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Computer Science, Information Systems, Life Sciences, Engineering, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in CSV/CSA within the pharmaceutical, biotechnology, or medical device industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ICH guidelines).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience applying a risk-based approach to validation, including CSA principles and GAMP 5 frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to lead validation projects and serve as a cross-functional SME and collaborative partner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, influence, and problem-solving skills; operates with a high degree of independence and a proactive, ownership-oriented mindset.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in a relevant field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with validation of both pure software systems (e.g., SaaS, cloud-based applications) and equipment with embedded or integrated software components (e.g., lab instruments, manufacturing equipment).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience contributing to the development or improvement of quality processes, quality systems, SOPs, or validation frameworks in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with Quality Management Systems (QMS) and electronic validation tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting regulatory inspections and audits.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$110,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$135,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$130,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$150,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5153184007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4639980007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5153184007,"updated_at":"2026-06-02T15:31:38-04:00","requisition_id":"888","title":"Manager, Data Integrity","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-02T15:31:38-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Serve as a hands-on team leader and subject matter expert supporting the company’s data integrity and quality management programs across GxP operations. This role is responsible for executing assessments, driving remediation, and maintaining compliance with applicable data integrity frameworks and standards (e.g., 21 CFR Part 11, Annex 11, , PIC/S), while contributing to QMS program execution and compliant data management practices.. The role is expected to interact with multiple internal departments in support of data integrity management initiatives.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute and support the implementation of data integrity policies, procedures, and program elements in alignment with global data integrity regulatory requirements; identify gaps and drive hands-on remediation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate cross-functional data integrity activities, serving as a working-level point of contact to maintain program momentum and support peer teams in adopting compliant data management practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct data integrity impact assessments, risk evaluations, and remediation plans; track progress and ensure timely closure of commitments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate data management, documentation, and record control practices across systems and formats; flag non-conformances and support corrective action.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess computerized systems, software, and equipment for compliance with 21 CFR Part 11, Annex 11, and related guidance; document findings and support risk-based computer system validation and assurance activities (CSV/CSA).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in and support data integrity audits and assessments; contribute to risk identification, gap analysis, and mitigation execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and execute CAPAs and process improvement initiatives to strengthen data integrity controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and mentor direct reports to support professional development and build data integrity team capability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support in the development and delivery of data integrity training materials; serve as a go-to resource for team members on ALCOA++ principles, regulatory requirements, and compliant data practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support regulatory inspections and partner audits as a subject matter contributor; prepare documentation and respond to data integrity inquiries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support ongoing data governance initiatives and compliant data management practices aligned with regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform additional duties as assigned to support objectives.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in science, engineering, information technology, computer science, data management, or a related technical discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of five (5) years of experience in the regulated pharmaceutical, biotechnology, or combination product industry, including demonstrated ability to coordinate or guide team-level work with increasing scope of responsibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive knowledge of GxP regulations, including GMP (FDA, EU, etc.), ICH guidelines, and ISO standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise with data integrity principles, data lifecycle management, and data governance frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience applying 21 CFR Part 11, Annex 11, and other relevant regulations and guidance governing data integrity and information security.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of information technology and data management systems, including system validation, security, and enterprise data governance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to coordinate cross-functional tasks, build effective peer relationships, and advance data integrity objectives through influence without formal authority.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented and solutions-focused, with demonstrated ability to manage competing priorities, escalate risks appropriately, and deliver on commitments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills; able to translate technical compliance requirements into clear, actionable guidance for cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience with the use of electronic document / quality management systems (EDMS / EQMS).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability for occasional business travel.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Certification or formal training in quality management, data integrity, data governance, or regulatory compliance (e.g., ASQ, ISPE, PDA, or equivalent).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$115,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$130,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5140229007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4633652007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5140229007,"updated_at":"2026-05-18T12:51:45-04:00","requisition_id":"865","title":"Manager, Marketing (HCP KAM)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-18T12:49:35-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Let’s do something amazing together! The HCP Key Accounts Manager(KAM) Marketing Manager at Arrowhead Pharmaceuticals will play a critical role in driving Arrowhead’s brand strategy and execution of materials on the cardiometabolic team serving patients living with Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG).\u0026amp;nbsp; Over time, this role could expand to cover additional indications and products in the Arrowhead cardiometabolic portfolio.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Manager will support the commercialization of Plozasiran for existing and future indications. The Manager will drive cross-functional collaboration with teams including HCP Marketing, Sales and KAM team leaders, Market Insights, Market Access, Regulatory, Medical Affairs and other key teams. This person will lead the development and execution of KAM (Key Account Manager)-focused tactics, EHR deliverables and support media strategy. This role requires a strong focus on personal and nonpersonal marketing execution for KAM audiences.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This individual should be detail-oriented, have excellent communication skills, feel comfortable working in a fast-paced environment and feel empowered to work both independently and collaboratively.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Manager will collaborate across teams to ensure consistent messaging, drive brand visibility, and lead marketing efforts that align with brand goals. Reporting to the Director of Marketing, you\u0026#39;ll drive brand awareness and contribute to Arrowhead’s market growth.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is base onsite 5x a week at Arrowhead’s Corporate Headquarters in Pasadena, CA.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Cross functional Collaboration\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain relationships with external partners, agencies, and vendors to ensure successful execution of marketing programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with KAM leadership, teams and training to develop and execute resources and strategic clarity for KAM team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support vendor/agency and print budget management and scope\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop effective relationships with medical, legal, regulatory and compliance teams to support overall brand and executional needs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Executional Excellence:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Content and Tool Development\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the execution and support omnichannel strategy for key accounts including RTE, CVA, Pop-health strategy decks, specialty pharmacy pathway pull-through decks, leave behinds, etc. in both personal and non-personal promotions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure promotional communications maintain consistency to brand guidelines and comply with regulatory guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support print material needs including printer relationship, KAM sales team needs and logistics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop pull-through marketing programs to support specialty pharmacy pathway activation and access milestones\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Director on messaging that bridges market access milestones with marketing messaging\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Market and Account Intelligence\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Monitor the industry, in-market tactical performance and competitive landscape and payer/account trends with ability to identify and translate into market optimizations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand EHR system foundation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;MLR Process\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure all materials go through proper MLR reviews and approvals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain compliance with all industry codes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Budget \u0026amp;amp; Planning\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage the KAM marketing budget, vendor relationships and project timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to brand planning with key account lens\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in marketing, communications, business, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of pharmaceutical marketing experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years managing KAM\u0026amp;nbsp; marketing initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional collaboration skills and the ability to lead strategic initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, leadership, prioritization and project management skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Veeva submission experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;EHR system understanding\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Marketing experience in the cardiometabolic and/or rare disease space\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Preferred product launch experience or creating marketing materials for newly developed KAM teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Health IT/systems professional experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Open to travel \u0026amp;gt;25%\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$120,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005300007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5138807007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4632950007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5138807007,"updated_at":"2026-05-15T10:39:27-04:00","requisition_id":"862","title":"Manager, Peer-to-Peer Engagement \u0026 Congress Programs","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-15T10:39:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Manager, Peer-to-Peer Engagement \u0026amp;amp; Congress Programs, is a key member of the Marketing team, responsible for executing peer-to-peer (P2P) programs and planning scientific congresses. The ideal candidate brings an understanding of the rare disease and cardiovascular landscapes, knowledge of HCP leaders in the therapeutic area, a track record of managing programs including MLR processes, overseeing agency/vendor relationships and the ability to collaborate cross-functionally.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in the office five days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Peer-to-Peer Program Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the development and execution of P2P initiatives including speaker bureau programs, advisory boards, and HCP-led educational events\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Align P2P programming with brand strategy and HCP targeting priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee speaker training logistics, field-based speaker programs, content development and review, and program performance tracking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all P2P activities are executed in full compliance with company policies, PhRMA guidelines, OIG regulations, and applicable laws\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage speaker program budget and provide line of sight to Sales leadership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Congress Planning \u0026amp;amp; Execution\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage planning and on-site execution of prioritized congresses and product theaters\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate cross-functional congress teams including Medical Affairs, Market Access, Sales, and external agencies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee congress HCP engagement programming\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop congress timelines, budgets, and post-event recaps\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary point of contact for congress vendors and association liaisons\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-Functional Collaboration \u0026amp;amp; Operations\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with Regulatory, Legal, and Medical Review (MLR) to ensure timely approval of all materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Medical Affairs to incorporate relevant data, review of content, and coordination of various engagement activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage agency relationships and hold external partners accountable to timelines, budgets, and quality standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track and report program spend against budget; identify opportunities for efficiency\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Requirements\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required, preferably in health sciences, business, or marketing, MBA or other advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of pharmaceutical or biotech marketing experience, with at least 2 years focused on HCP engagement, P2P programs, or congress operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with KOLs and managing speaker bureau programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with Veeva Vault or similar MLR review platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Agency management experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in rare disease, cardiovascular, specialty, or orphan drug marketing strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage multiple complex projects simultaneously with strong attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of PhRMA Code, OIG guidelines, and pharmaceutical promotional compliance requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills; ability to influence without authority\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel up to 30–40%, including weekends for congress coverage\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$120,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005300007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5030663007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4582479007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5030663007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"718","title":"Manager, Quality Control (2nd Shift)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-01-21T16:25:57-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position falls within the Quality Control structure, under the Quality Organization. The Quality Control Manager will manage a team of chemists and help to support the analytical testing of pharmaceutical raw materials, in­ process manufacturing samples, finished drug substances and drug product, and stability sample testing activities for new drug substances and drug products while carrying out a leadership function.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Quality Control Manager will manage, and support testing required for clinical and commercial programs in the GMP QC laboratories at Arrowhead Verona site. The Manager is expected to be proficient in several analytical techniques and will be capable of making independent scientific decisions. The position requires the ability to lead and mentor new chemists who are new to the industry. May require occasional extended hours based on operational needs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2nd shift work hours are 1 pm – 11:30 pm, Monday - Thursday, and includes a 10% shift differential.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Leadership\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide daily oversight of QC testing activities to ensure accurate, timely release and stability testing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage sample scheduling, resource planning, and prioritization to support program timelines and ensure operational continuity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides leadership and guidance to a team of QC chemists, ensuring their professional growth and development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trains and mentors QC chemists\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sets clear performance expectations, provides regular feedback, and conducts performance evaluations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fosters a collaborative and inclusive work environment that encourages teamwork, creativity, and innovation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend and contribute to regular leadership meetings between cross-functional departments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Scientific/Laboratory\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Fully knowledgeable of cGMP requirements and ICH guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works independently to meet project timelines and deliverables with minimal supervision to no supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates with Analytical Development on procedural method transfers and may participate in the execution of method validation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains and continuously develops proficiency with various analytical instrumentation theory and practice.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute training requirements for assigned SOPs and participate in department specific training\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Is a subject matter expert in technical aspects of both instrumentation and workflow management and\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identifies and troubleshoots analytical method issues with instrumentation, general chemistry, test methodology and sample\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicates laboratory testing issues or challenges to senior laboratory\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead, author, and drive timely closure of laboratory non-conformances, including atypical results, Out‑of‑Specification (OOS), Out‑of‑Trend (OOT), and deviations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses clear written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Calibration, maintenance, and troubleshooting of analytical equipment in collaboration with metrology.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Acts with a high degree of judgement to make sound, scientific decisions and serve as a back-up to Senior Laboratory\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S or M.S in chemistry or related field required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;M.S. with 5+ years of relevant experience, B.S. with 7+ years of relevant experience in GMP QC laboratory, with 5+ years in a leadership role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise with analytical instrumentation theory and practice.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, UV-Vis spectroscopy, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in analyst training on instrumentation as\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pharmaceutical experience required; experience with oligonucleotide testing strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience with pharmaceutical drug substance, drug product and in-process validation and testing preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience with compendial methods: pH, osmolality, appearance, UV, endotoxin, bioburden, environmental monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of data integrity, GxP, and regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Language Skills: Ability to read, analyze and interpret SOPs, test methods, procedural guides and associated technical documents. Ability to write in a clear and concise manner. Ability to effectively present/communicate information and respond to questions from management, peers and colleagues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mathematical Skills: Must be able to perform complex mathematical calculations, compute ratios, rate, and percent. Must be able to draw and interpret graphs and charts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reasoning Skills: Must be able to solve practical problems. Must be able to interpret a variety of instructions furnished in written, oral, diagram or schedule form.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communication Skills: Ability to interact and interface with department management across various disciplines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other Skills and Abilities: Must be able to work with people at various levels of the organization. Must have basic knowledge of computers and PC\u0026#39;s. Ability to use windows-based software including MS Office and chromatography data collection software.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$110,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$130,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=4917284007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4520991007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":4917284007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"607","title":"Manager/Sr. Manager, Biostatistics","company_name":"Arrowhead Pharmaceuticals ","first_published":"2025-09-23T18:49:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a stellar biostatistician to join our rapidly growing biometrics team to support clinical studies across Arrowhead’s expanding portfolio. As an internal expert in biostatistics, you will provide technical leadership and biostatistical input to closely collaborate with other functional teams at Arrowhead, including Clinical Development and Operations, Regulatory, Commercial, Program Management and others.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide sound statistical and operational input, including study and program design, writing of the protocol sections, statistical analysis plans (SAP), clinical study reports (CSR), regulatory documents or scientific publications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with cross functional teams to provide strategic biostatistics input to support entire drug development process; ensure statistical integrity of all key deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide statistically sound scientific methodology for study design and data analysis input to meet project objectives in accordance to regulatory guidance and industry standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with the programming and data management functions to ensure appropriate data collection and reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership in evaluating alternative or innovative methods of study design and analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in efforts to identify, develop and implement departmental standards, applications, processes and training\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversees statistical and programming deliverables by CROs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in identifying consultants and the selection of service providers\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in Biostatistics/Statistics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of relevant experience in pharmaceutical or biotechnology drug development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding and experience with various aspects of a clinical development life-cycle, leading up to regulatory submission and post-approval activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience interacting with and overseeing biometrics services of CRO vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in the use of statistical software including SAS and R at minimum; familiarity with East and Spotfire\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of pharmaceutical clinical development processes and ability to effectively apply technical principles and methods to clinical drug development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective in communication and team collaboration, influencing across different functional lines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of cross-functional department functions/roles within a drug development company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Understanding of regulatory guidelines related to submission of datasets using CDISC, development of SDTM and ADaM specifications\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$145,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$190,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005292007,"name":"Biostats \u0026 Data Management","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5071984007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4601840007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5071984007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"786","title":"Process Validation Engineer","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-06T11:28:18-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly skilled and motivated Process Validation Engineer with a strong background in Good Manufacturing Practices (GMP) to join our team. This individual will be responsible for drafting, reviewing, and overseeing the execution of process and cleaning validation documentation. The ideal candidate will have a minimum of 8 years of experience in GMP validation or related fields, with at least 3 years of GMP manufacturing experience preferred.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Draft and review process validation and cleaning validation protocols and reports, ensuring compliance with GMP regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and manage the execution of manufacturing validation activities, ensuring timelines and quality standards are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams to ensure validation strategies align with production requirements and regulatory guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical support to manufacturing during validation and qualification activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and assess risks, proposing corrective actions and improvements to enhance validation processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with all applicable regulatory requirements, including FDA, EMA, and ICH guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve validation data and documentation to ensure accuracy and regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in audits and inspections, providing validation documentation and responding to inquiries from regulatory agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide training and mentorship to employees on validation processes and GMP standards.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8 years of experience in GMP validation or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of process and cleaning validation activities, including test methods, execution, and data analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent technical writing skills with high attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent problem-solving skills and attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills to effectively interact with internal teams, management, and regulatory bodies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with regulatory submissions and/or inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work across teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in drafting and reviewing validation protocols and reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of GMP regulations, validation principles, and industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a pharmaceutical or biopharmaceutical manufacturing environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;3 years of GMP manufacturing experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Six Sigma or Lean certifications\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$90,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$120,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5152120007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4639484007,"location":{"name":"Madison, Wisconsin, United States"},"metadata":null,"id":5152120007,"updated_at":"2026-06-01T17:27:27-04:00","requisition_id":"884","title":"Project Coordinator II, Discovery Chemistry","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-01T17:27:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Chemistry Project Coordinator will support the development of investigational drugs in the Arrowhead pipeline by working with Chemistry department team leads on custom outsourcing projects. In this position, the Project Coordinator will collaborate with chemistry leads to define deliverables and monitor timelines through coordination and communication between internal and external collaborators. They will act as the primary contact with third-party vendors. They will also collaborate with department leadership to plan and track project budgets and other departmental support tasks.\u0026amp;nbsp;The ideal candidate will have excellent communication skills and be detail-oriented, responsive, collaborative, and have a background in chemistry or biotechnology.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborates with chemistry leads to initiate, support, and manage outsourced custom synthesis projects to support drug research and development\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Draft and edit outsourcing (OS) proposals and facilitate the OS approval process\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitors progress and communicates project status, activities, timeline updates, and risk assessments to leadership and project stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review progress reports and related analytical data; consult with chemistry leads to provide technical feedback and otherwise facilitate communication between internal and external parties; addresses questions and concerns throughout the project; coordinates shipment process and deliveries\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a liaison between company and third parties to facilitate communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide regular status reports to senior management\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinates purchase requests and approvals, confirms delivery and related invoice approval\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Department Management and Finance teams on annual budget planning and quarterly updates and revisions, as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures compliance with federal, state, local, industry, contractual, and company regulations, standards, specifications, and best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs other related duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biopharmaceutical related area, which may include chemistry, biochemistry, chemical engineering, biotechnology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of pharmaceutical or scientific industry and project planning experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with MS programs including Excel, Word, and PowerPoint.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong verbal and written communication skills and ability to work in a cross-functional environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid organizational skills with ability to adapt to changing priorities and deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills and attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent time management skills with a proven ability to meet deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to prioritize multiple tasks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough understanding of or the ability to quickly learn about the project or product being developed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Microsoft Office applications\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Background in chemistry or related experience, experience with oligonucleotide therapeutics, peptides and/or biologics a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing vendors and partner relationships\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$60,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$75,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005284007,"name":"Discovery Chemistry","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5149956007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4638434007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5149956007,"updated_at":"2026-05-29T11:24:42-04:00","requisition_id":"878","title":"Project Coordinator II, Stability Quality Control","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-29T11:24:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Stability Coordinator is responsible for assisting in the oversight and management of Arrowhead’s stability program. Key responsibilities of this position include preparing stability samples for study initiation, tracking timepoint pull dates, performing sample pulls, and maintaining testing data forms and reports. The Stability Coordinator will provide study documentation oversight to ensure that study reports are complete and accurate. This position will communicate with contract vendors to coordinate analytical testing and sample storage and is responsible for the reconciliation and disposition of stability samples upon completion of studies.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work cross-functionally with Manufacturing to ensure release and stability samples are received and transferred to the appropriate testing lab(s).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Authoring, review, and revision of Stability documents including protocols, work instructions, and Stability reports, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform stability study initiations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in maintaining stability timepoint pull schedules and perform timepoint sample pulls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Management of samples including reconciliation of inventory, sample location, and distribution of samples to testing lab(s).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain communication with external testing laboratories or storage facilities to coordinate shipments and sample analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in routine maintenance of stability chambers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the management of stability program data and reports, maintain program study folders, and compile and interpret data for internal and external stability studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help Ensure that reported stability testing results are complete, accurate, and documented per ALOCOA++ standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the set down and management of internal and external retain and reserve samples.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work cross-functionally to provide oversight of stability processes and improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Chemistry (or related scientific field) with 2+ years’ relevant experience (pharmaceutical CMO/CRO).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with MS programs including Excel, Word, and PowerPoint.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong verbal and written communication skills and ability to work in a cross-functional environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid organizational skills with ability to adapt to changing priorities and deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of cGMP and cGLP guidelines for contract manufacturing and analytical laboratories and ICH/FDA guidance documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with stability programs and sample handling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;LIMS system experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Smartsheet, or similar.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$70,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$80,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5139947007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4633529007,"location":{"name":"Madison, Wisconsin, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5139947007,"updated_at":"2026-05-18T10:31:18-04:00","requisition_id":"864","title":"Purchasing Analyst (6-Month Temporary Assignment)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-18T10:31:18-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Purchasing Analyst plays a key role in procuring materials and goods to support the Company’s operations. This position collaborates closely with both internal stakeholders and external vendors to source goods, materials, and services. Responsibilities include supporting procurement activities such as price negotiations, vendor management, and spend analysis to ensure cost-effective and timely purchasing decisions and order placement.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is full-time onsite, 5 days a week in Madison or Verona, WI.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with assigned departments to understand purchasing needs and support sourcing, vendor selection, and purchasing decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recommend preferred suppliers and identify vendor consolidation opportunities to improve efficiency and cost effectiveness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist internal business partners with purchase requests; compile and process purchase requisitions and purchase orders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with internal stakeholders to conduct periodic purchasing and ordering reviews\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and participate in vendor business reviews to evaluate performance and service levels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Place orders, track deliveries, and confirm receipt of off-the-shelf goods and materials from external suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify and mitigate purchasing, delivery, and lead-time issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support contract negotiations, pricing discussions, and commercial terms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with the purchasing team to drive process improvements and enhance overall team efficiency and effectiveness\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Associate degree or active progress toward a bachelor’s degree\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Intermediate proficiency with Microsoft Outlook and Excel\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and time-management abilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-starter with a proactive work ethic\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, written, and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level of accuracy and attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to prioritize responsibilities and manage multiple timelines\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience using ERP system\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$55,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$65,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005296007,"name":"Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null},{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5149376007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4638111007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5149376007,"updated_at":"2026-05-28T17:00:48-04:00","requisition_id":"875","title":"Quality Assurance Specialist II - External Quality","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-28T17:00:48-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The purpose of this position is to provide quality assurance support to programs utilizing contract development, manufacturing, and testing organizations. The incumbent will review vendor documentation and perform lot disposition per applicable quality agreements as well as capture quality data and generate metrics for vendors. The incumbent will be expected to interact with internal departments as well as multiple contract organizations to support ongoing commercial, pre-clinical and clinical development programs at Arrowhead Pharmaceuticals, Inc.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Interact with personnel companywide to obtain the necessary information and details to provide quality assurance support of development, clinical, and commercial programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve vendor generated documentation, including but not limited to, executed batch records, testing records, certificates of analysis (CoA), labels, protocols, and reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with vendors on quality events and non-conformances as outlined in the applicable quality agreement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform lot disposition and generate certificates of compliance (CoC) as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with preparation, update, review, and routing of Arrowhead procedural documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Scan and upload executed documents to the EDMS, properly categorize within the system, and route for verification/approval.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with QA duties as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 3 years of quality assurance or similar experience in a biotech or pharmaceutical development, manufacturing, or contract manufacturing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of GMP, GCP, and/or GLP regulations as well as ICH and FDA guidance documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, verbal, and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to consistently communicate with external parties in a professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to follow company procedures, work instructions, and policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent attention to detail and organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with minimal supervision as well as manage priorities within a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with use of an electronic document management system in a regulated environment is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office programs, and Smartsheet.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$70,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$85,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5143782007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4635323007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5143782007,"updated_at":"2026-05-21T01:05:03-04:00","requisition_id":"868","title":"Scientist I, CMC Process Development","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-21T01:05:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A Scientist I, Late Phase Process Development works within the CMC department on small molecule and conjugation chemistry to generate knowledge and documents to support late phase process development and regulatory filings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee and perform experiments for late phase process development of API and regulated materials, including process improvement, impurity identification, and fate and purge studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze and interpret experimental technical data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with internal and external teams to manage the determination, supply, and specifications of materials for Arrowhead’s late phase drug substance programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain knowledge of process and project history as well as process development and regulatory issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Regulatory Affairs in the preparation of regulatory documents, including CTAs, IMPDs, NDAs, and MAAs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Make oral presentations to scientists and management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Guide, mentor and develop chemists across the team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support talent acquisition efforts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify growth opportunities for team members to reach their full potential\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with other department members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recommend new ideas, synthetic routes, and technologies to support departmental goals\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Master’s Degree in Chemistry with at least 5 years work experience or Bachelor’s Degree in Chemistry with at least 8 years equivalent industry work experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge in synthetic chemistry and analytical technology, hands-on experience in syntheses and development of small molecule and large molecule drug candidates\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong track record of scientific publication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with cGMP manufacturing and pharmaceutical regulatory compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience working with or within CDMOs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$85,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$95,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005288007,"name":"Chemistry Manufacturing \u0026 Controls","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5161267007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4643938007,"location":{"name":"San Diego, California, United States"},"metadata":null,"id":5161267007,"updated_at":"2026-06-10T14:24:27-04:00","requisition_id":"893","title":"Scientist I, Histology","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-06-10T14:24:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Scientist I is a key contributor to the Histotechnology team within the Biology Department. In partnership with the Histology Manager and cross-functional study teams, this role supports preclinical drug-development programs by planning and executing tissue collection strategies; processing, embedding, and sectioning specimens; performing histologic and immunohistochemical stains; and summarizing results for study teams. The Scientist I execute a broad range of routine and non-routine histology methods with consistent quality and reproducibility, communicates clearly with stakeholders, and exercises appropriate independence in day-to-day decision making.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is onsite 5 days a week in San Diego.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Study Support \u0026amp;amp; Communication — Translate study requirements into practical histology work plans (sampling schemes, section levels, stain menus, controls, timelines) and present interim results to program stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sample Handling \u0026amp;amp; Documentation — Coordinate specimen receipt, accessioning, labeling/barcoding, and chain-of-custody; maintain complete, accurate, audit-ready records in LIMS/ELN or designated systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Processing, Embedding \u0026amp;amp; Sectioning — Perform routine automated tissue processing and paraffin embedding; microtome and cryosection a range of animal tissues at 5–7 µm; complete re-cuts and serial levels as needed with minimal artifacts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Staining \u0026amp;amp; Assay Execution — Execute H\u0026amp;amp;E, special stains, and IHC/IF on manual and automated platforms, including antigen retrieval, antibody titration, protocol design, and troubleshooting; contribute to method validation (e.g., RNAscope/miRNAscope, multiplex IHC/IF).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Microscopy, Imaging \u0026amp;amp; Reporting — Perform microscopic QC, identify representative regions, and use imaging/slide scanning as available to support digital pathology; compile clear data summaries and presentations for study leads.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality, Safety \u0026amp;amp; Continuous Improvement — Adhere to SOPs and applicable quality expectations; follow biosafety and chemical-safety procedures; participate in deviations/CAPA as appropriate; contribute to team-based improvements (e.g., 5S/Lean).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Instrumentation \u0026amp;amp; Inventory — Operate and perform routine maintenance/calibration checks for microtomes, cryostats, stainers, printers, microscopes; track reagents/antibodies and coordinate ordering and lot qualification.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS or MS degree in Cell Biology, Molecular Biology, Biochemistry, or related discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;BS with a minimum of seven (7) years relevant histology laboratory experience or a MS with 3+ years of academic/industry laboratory experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with microtomes, cryostats, cassette/slide printers, automated slide stainers, and microscopes; practical knowledge of tissue composition.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in IHC/IF staining, protocol development, validation, and troubleshooting (including antibody titration and antigen retrieval).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project- and time-management skills with the ability to manage multiple studies and deadlines; effective written and verbal communication.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced computer skills (e.g., Excel and imaging software);\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to process valuable/delicate samples and to prepare tissue for pathologist interpretation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Degree from an accredited Histotechnology program, HT or HTL(ASCP) certification\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience validating RNAscope/miRNAscope and multiplex IHC/IF across multiple tissues/species.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with LIMS/ELN.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with digital pathology and whole-slide imaging\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$115,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$125,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005285007,"name":"Biology","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5110487007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4619455007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5110487007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"836","title":"Scientist I, Quality Control","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-16T10:31:07-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position is within the Quality Control structure, under the Quality Organization. A Scientist I, Quality Control will support the analytical testing of Environmental monitoring samples, pharmaceutical raw materials, in­ process manufacturing samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Senior Scientist I will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Senior Scientist I is expected to be proficient in several analytical techniques and will be capable of making independent scientific decisions. The position also requires the ability to lead and mentor co-workers. This position reports to QC Laboratory Management.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Fully knowledgeable of cGMP requirements and ICH guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works independently to meet project timelines and deliverables with minimal supervision to no supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with various analytical instrumentation theory and practice\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Executes training requirements for assigned SOPs and participates in department specific training modules.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation as\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs analyses in a timely and efficient manner to support ongoing prioritized studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works closely with other department personnel for efficient project execution and timely/accurate deliverables while building a relationship with respect and communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trains and mentors co-workers (analysts)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Shows initiative and interest in mastering new techniques and tests\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to track/trend data and interpret degrative changes to the product on stability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Uses stability tracking software as a repository generated results (data entry, review and approval).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Owns and leads scientific technical discussions and brainstorming sessions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identifies and troubleshoots analytical method issues with instrumentation, general chemistry, test methodology and sample product\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicates laboratory testing issues or challenges to laboratory management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains a clear, concise, and accurate notebook\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs technical data review on data acquired by other QC analysts as applicable\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drafts technical documents such as COAs, investigations, deviations, and CAPAs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses excellent written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Embraces cGMP and ICH requirements for all associated work\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works cooperatively in a team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates a high attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Calibration, maintenance, and troubleshooting of analytical equipment with little to no guidance from management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely makes sound, scientific decisions independently and serves as a back-up to Laboratory Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates enduring flexibility and understanding with changing priorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fully knowledgeable of cGMP and ICH laboratory requirements and operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$90,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$108,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=4958682007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4544574007,"location":{"name":"San Diego, California, United States"},"metadata":null,"id":4958682007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"630","title":"Scientist/Senior Scientist, Antibody Engineering","company_name":"Arrowhead Pharmaceuticals ","first_published":"2025-10-27T11:14:58-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated and skilled Molecular Biologist to join our dynamic research team in Discovery Chemistry,. The successful candidate will play a key role in antibody engineering to support platform development and drug delivery initiatives. This position requires extensive hands-on experience in phage display, antibody engineering, and antibody characterization, supported by a strong foundation in molecular biology.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design and construct mutant phage libraries for antibody affinity maturation or humanization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform molecular cloning, mutagenesis, antibody gene assembly, and expression vector design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Express and purify recombinant antibodies using bacterial and mammalian expression systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform binding, specific and in vitro functional assays.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional project teams to advance lead antibodies through drug development stages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate documentation and present findings at internal meetings.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ph.D. in Biology, Biochemistry, Molecular Biology, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with phage display technology for antibody engineering.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in molecular cloning, PCR, and mutagenesis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with antibody expression and purification using E. coli, HEK293, and CHO systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills, with the ability to troubleshoot experiments independently.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent record-keeping, communication, and collaboration skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to adapt to fast pace and evolving research priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track record of scientific productivity, including peer-reviewed publications, conference presentations, or patents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Additional experience in molecular biology and/or antibody discovery is highly desirable\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Industry or postdoc experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$120,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$150,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005284007,"name":"Discovery Chemistry","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5112662007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4620459007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5112662007,"updated_at":"2026-06-03T15:53:39-04:00","requisition_id":"839","title":"Senior Commercial Coordinator","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-17T12:30:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals is seeking a highly organized, proactive, and detail-oriented Commercial Coordinator to provide critical support to the Commercial team. This role is instrumental in ensuring the seamless operation of all Commercial teams within the Cardiometabolic Franchise and beyond, delivering high-level administrative assistance, and contributing to a collaborative and efficient work environment.\u0026amp;nbsp; The ideal candidate is a skilled communicator, thrives in a fast-paced setting, and excels at managing multiple priorities with precision and professionalism. This role reports to Sr VP, Global Cardiometabolic Franchise.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in office 5 days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contract Coordination/Vendor Management: Assist with the preparation, review, tracking and organization of contracts, purchase orders, ensuring timely execution and compliance. Ability to communicate professionally with vendors and KOLs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document Management: Organize and maintain confidential documents, files, and reports for swift access and secure handling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel \u0026amp;amp; Congress Management: Coordinate and manage domestic and international travel arrangements for various congresses, including event logistics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Meeting Planning: Coordinate meeting logistics, including room and venue bookings, catering, and travel arrangements, preparing agendas to create a seamless experience for participants.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Event Planning: Support the planning and execution of commercial events, off-site meetings and team activities, fostering engagement and collaboration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Budget Tracking: Tracking department budget and providing leaders with updates. Tracking and managing invoices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Calendar Oversight: Ability to schedule meetings and appointments in Outlook with extreme accuracy and prioritization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Onboarding: Support recruitment of new hires by scheduling interviews and requesting access to/setting up necessary systems needed for onboarding.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Special Projects: Contribute to special projects with a focus on delivering high-quality results within deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team Collaboration: Willingness to pitch in where needed, may include providing assistance at company events and meetings.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5 years of experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Technical Proficiency: Strong skills in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint), Concur, and experience using contract management systems (e.g. Agiloft).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communication: Strong written and verbal communication skills; ability to interact effectively and professionally with all levels of the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-Oriented: Outstanding organizational and time management skills with meticulous attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adaptability: Ability to thrive in a dynamic environment with shifting priorities, responding to urgent requests as needed, even outside standard hours.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Confidentiality: Proven ability to handle sensitive information with discretion and integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive attitude: Approachable, reliable, willingness to help, problem-solver.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Additional Qualities: Resourcefulness, creativity, a sense of urgency and a proactive mindset are highly valued.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous Commercial/Marketing and/or Biopharmaceutical support experience.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$95,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$120,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005300007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5124162007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4620459007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5124162007,"updated_at":"2026-06-03T15:53:39-04:00","requisition_id":"839","title":"Senior Commercial Program \u0026 Operations Specialist","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-29T13:59:49-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals is seeking a highly organized, proactive, and detail-oriented Senior \u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Commercial Program \u0026amp;amp; Operations Specialist \u0026lt;/span\u0026gt;to provide critical support to the Commercial team. This role is instrumental in ensuring the seamless operation of all Commercial teams within the Cardiometabolic Franchise and beyond, delivering high-level administrative assistance, and contributing to a collaborative and efficient work environment.\u0026amp;nbsp; The ideal candidate is a skilled communicator, thrives in a fast-paced setting, and excels at managing multiple priorities with precision and professionalism. This role reports to Sr VP, Global Cardiometabolic Franchise.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Pasadena, California, with an expectation to be in office 5 days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contract Coordination/Vendor Management: Assist with the preparation, review, tracking and organization of contracts, purchase orders, ensuring timely execution and compliance. Ability to communicate professionally with vendors and KOLs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document Management: Organize and maintain confidential documents, files, and reports for swift access and secure handling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel \u0026amp;amp; Congress Management: Coordinate and manage domestic and international travel arrangements for various congresses, including event logistics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Meeting Planning: Coordinate meeting logistics, including room and venue bookings, catering, and travel arrangements, preparing agendas to create a seamless experience for participants.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Event Planning: Support the planning and execution of commercial events, off-site meetings and team activities, fostering engagement and collaboration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Budget Tracking: Tracking department budget and providing leaders with updates. Tracking and managing invoices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Calendar Oversight: Ability to schedule meetings and appointments in Outlook with extreme accuracy and prioritization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Onboarding: Support recruitment of new hires by scheduling interviews and requesting access to/setting up necessary systems needed for onboarding.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Special Projects: Contribute to special projects with a focus on delivering high-quality results within deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team Collaboration: Willingness to pitch in where needed, may include providing assistance at company events and meetings.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5 years of experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Technical Proficiency: Strong skills in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint), Concur, and experience using contract management systems (e.g. Agiloft).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communication: Strong written and verbal communication skills; ability to interact effectively and professionally with all levels of the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-Oriented: Outstanding organizational and time management skills with meticulous attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adaptability: Ability to thrive in a dynamic environment with shifting priorities, responding to urgent requests as needed, even outside standard hours.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Confidentiality: Proven ability to handle sensitive information with discretion and integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive attitude: Approachable, reliable, willingness to help, problem-solver.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Additional Qualities: Resourcefulness, creativity, a sense of urgency and a proactive mindset are highly valued.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous Commercial/Marketing and/or Biopharmaceutical support experience.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$95,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$120,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005300007,"name":"Commercial","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5106851007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4617591007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5106851007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"834","title":"Senior Manager, Client Quality Management","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-04-13T16:32:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Manager, Client Quality Management oversees and manages quality-related client and partner interactions, ensuring compliance with internal quality standards and procedures, applicable contracts, license agreements, and Quality Agreements, as well as pharmaceutical industry regulations. This role serves as a key liaison between Arrowhead partners/clients and internal stakeholders to manage notifications and support the resolution of quality related issues, manage expectations, and assist with the transfer of required documentation for review and approval.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead client and partner quality management activities, ensuring alignment with applicable licensing agreements, contracts, and quality agreements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the client notification process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee resolution of client quality events, including deviations, change controls, CAPAs, and investigations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and support quality and Alliance/program/project management with the transfer of quality related deliverables, including batch release, document approvals, and other documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and\u0026amp;nbsp;maintain\u0026amp;nbsp;strong client relationships to enhance transparency and collaboration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with and represent Quality at internal cross-functional meetings to support client management.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in the life sciences fields or equivalent work experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7 years of experience in pharmaceutical or other related regulated industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of\u0026amp;nbsp;GxPs including, but not limited to, GMP, GDP, GLP, and GCP, along with global regulatory expectations, and pharmaceutical quality systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated client collaboration experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, negotiation, and problem‑solving skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality experience within a regulated industry preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated\u0026amp;nbsp;leadership and project management abilities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$145,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5131591007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4629252007,"location":{"name":"San Diego, California, United States; Verona, Wisconsin, United States"},"metadata":null,"id":5131591007,"updated_at":"2026-05-07T11:02:56-04:00","requisition_id":"855","title":"Senior Manager, Clinical Supply Management","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-07T11:02:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is responsible for the planning and management of investigational medicinal product (IMP) needed to ensure uninterrupted patient dosing for assigned clinical studies.\u0026amp;nbsp; This role will create and maintain study forecast and supply plans, develop clinical labels, execute packaging and labeling activities, manage distribution, inventory, and returns \u0026amp;amp; reconciliation of clinical studies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Furthermore, this role will be required to work closely with clinical contract manufacturers (CMOs) worldwide, as well as other cross functional partners to ensure supply continuity with optimal cost and quality. You will drive the evolution and implementation of new platforms, systems and processes that enable greater operational efficiency, accuracy, and utilization of the product portfolio.\u0026amp;nbsp; You will use your manufacturing and PM experience as well as partner relationships to optimize the overall supply chain helping to achieve the goal of delivering Arrowhead’s pipeline to patients.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in onsite with an expectation to be in the office five days a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with Clinical Operations, Manufacturing, Regulatory Affairs, and Quality Assurance to forecast, plan, and execute IMP supply plans including IMP utilization, labeling and packaging, inventory control, and depot management for assigned clinical studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, update, and adapt clinical supplies distribution plans based on program and study timelines, trial design, clinical program changes, recruitment, geography, and manufacturing schedules.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop plans for ancillary supply sourcing and liaise with CMC team to ensure ancillary compatibility with IMP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage SOPs, work instructions, processes, systems, and forms governing clinical supplies management in alignment with industry standards and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with cross functional team including Clinical Operations and Quality Assurance to manage IMP shelf-life extensions, temperature deviation management, product complaints, and associated investigations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify potential supply chain vendors and review proposals contributing to the selection process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee aspects of Arrowhead’s global network of clinical CMOs supporting clinical drug supply. Scope of work includes management of drug from the release of Drug Product (DP) at the filling site through release of Final Packaged Goods (FG) at the label/pack site (or depot in some cases); scheduling and oversight of label/pack execution activities at the label/pack site; and ensuring the necessary materials and components are available for execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with internal cross-functional teams to determine manufacturing requirements. Drive contract manufacturer capability and capacity to enable on-time and predictable delivery of packaged clinical product.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the operational pack activities (schedule, timelines, etc.) of the CMO ensuring program cost, quality, metrics, delivery, and technology objectives are met as well as manage the partner performance to achieve them. Proactively intercede if goals and timelines are jeopardized, communicating to appropriate stakeholders as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with key stakeholders in the preparation for Requests for Quotes (RFQs), Statements of Work (SOW) and negotiate supply agreements for clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the manufacturing outsourcing team leader on cross-functional teams as requested in support of clinical finished good packaging.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support QA in establishing QA agreements with all CMO’s and assuring that Product Specific Requirements (PSR’s) are established before projects are initiated.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply advanced theory, technical principles, expert judgment, and cross-functional expertise to independently address a broad range of complex problems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and champion process improvement solutions to complex issues with inter-organizational impact.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;4-year college degree (relevant discipline preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough understanding of GMP, GCP, and ICH standards governing IMP labeling,\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;packaging, and global distribution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong vendor management skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to proactively perform and complete duties with minimal supervision in an accurate and timely manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in MS Office (Word, Excel, and PowerPoint) and Smartsheet\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a team or independently.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective interpersonal, written, and verbal communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to critically evaluate and prioritize job tasks and the impact on overall study execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively collaborates with cross-functional team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional organizational skills with the ability to multi-task and prioritize.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 6-8 years in a clinical supply chain management and/or PM role; additional industry experience desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with electronic interactive response technologies for inventory management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;ERP experience desired.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$140,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$160,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$180,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null},{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5130292007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4628653007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5130292007,"updated_at":"2026-05-06T10:41:35-04:00","requisition_id":"853","title":"Senior Manager, CMC Regulatory Affairs","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-06T10:40:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Sr Manager Regulatory CMC ensures efficient and compliant management of regulatory change control and post-approval activities. Supporting diverse modalities—including small molecules, biologics, and external manufacturing sites—the role employs an agile approach to drive standardization, scalability, and sustainability.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position leverages ICH Q12 principles to streamline post-approval change management. The Sr Manager Regulatory CMC will have good experience with global HA requirements along with an understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support. The Sr Manager has a proven ability to understand and communicate regulatory strategy for drug development, registration, and post-market support teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead post-approval change management activities, including record evaluations and regulatory submissions (considering possible strategic bundling of changes), ensuring compliance with global requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply science- and risk-based approaches, guided by ICH Q12 principles, to assess and implement post-approval changes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Explore and implement automation technologies to increase efficiency and ensure repeatability in change control and regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide centralized regulatory support for manufacturing sites, including external partners, covering small molecules and biologics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with external manufacturing sites and suppliers to align change control processes with global regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure site compliance with global regulatory requirements by evaluating and prioritizing changes based on risk and scientific rationale.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate alignment between CMC teams and global Regulatory CMC on post-approval strategies and activities and represent global Regulatory CMC in cross-functional Change Review meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement streamlined workflows for regulatory change control, leveraging digital tools and automation to minimize delays and maximize impact.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA Degree in a Scientific Discipline,\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with CMC Life Cycle Management Systems (such as Veeva Registrations)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of overall biopharmaceutical/device industry experience with 5+ years of direct Regulatory CMC experience required. This can include experience leading a major variation/amendment, or supporting an initial NDA/BLA.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong practical experience with global HA requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to understand and communicate regulatory strategy to drug development, registration, and post-market support teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to develop global regulatory strategy recommendations based on precedents and other regulatory intelligence as well as regulations and guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to deal with issues of critical importance with minimal oversight. Exercises good judgment in elevating and communicating actual or potential issues to line management.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced Degree (M.S., Ph.D., etc.) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$140,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$170,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005297007,"name":"Regulatory","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5079269007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4605142007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5079269007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"803","title":"Senior Manager, GxP Systems \u0026 Validation","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-13T16:29:02-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Manager GxP Systems \u0026amp;amp; Validation provides strategic and operational leadership for GxP-regulated computerized systems across their full lifecycle. This role is accountable for governance, validation strategy, inspection readiness, and compliant system administration, ensuring alignment with global regulatory requirements (FDA, EMA, MHRA, ICH) and evolving industry standards (GAMP 5, CSA).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This leader serves as a key partner to Manufacturing, Quality, CMC, CSA and Compliance, GLP Operations, and external vendors, driving scalable compliance frameworks while enabling business agility. The role combines system ownership and administration, validation project management, and organizational oversight to ensure enterprise-wide data integrity and computerized system compliance.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Strategic Leadership \u0026amp;amp; Governance\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain governance frameworks for GxP computerized systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define validation strategies aligned with GAMP 5 and CSA principles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support modernization initiatives (e.g., SaaS adoption, cloud validation, CSA transition)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as system owner and system administrator for critical GxP platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain validation and system lifecycle policies and standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates in continuous improvement of validation methodologies, templates, and risk-based approaches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide compliance guidance to executive leadership and functional heads\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;System Lifecycle Oversight\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee administration and compliant operation of GxP systems (Laboratory systems, LIMS, MES, EDMS, enterprise SaaS platforms)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure systems remain validated, secure, and audit-ready throughout implementation, upgrades, and decommissioning\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Approve system configurations, changes, and access governance frameworks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure robust data integrity controls in accordance with ALCOA+ principles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor system performance, audit trails, cybersecurity controls, and vendor compliance\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Validation Program Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead enterprise validation initiatives across multiple concurrent projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee development and approval of validation deliverables (URS, Risk Assessments, IQ/OQ/PQ, Traceability, Summary Reports)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure appropriate application of risk-based validation and CSA methodologies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage validation master planning and resource allocation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of regression testing and revalidation strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure validation documentation supports global inspection readiness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as SME during regulatory inspections and internal audits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee remediation efforts related to audit findings, deviations, and CAPAs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain awareness of evolving global regulatory expectations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Project \u0026amp;amp; Vendor Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead cross-functional teams across CMC, Quality, IS\u0026amp;amp;I, Manufacturing, Engineering, GLP Operations, and external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee third-party vendors and validation consultants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage budgets, timelines, risks, and resource planning for validation programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive issue resolution and escalation management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure vendor deliverables meet compliance and quality standards\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;People \u0026amp;amp; Organizational Development\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead, mentor, and develop validation and system administration staff\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish performance expectations and competency development plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build scalable team capabilities to support business growth\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences, Engineering, IT, or related discipline (advanced degree preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in GxP computerized systems and validation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years in a leadership or program management role\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in CSV/CSA, GAMP 5, 21 CFR Part 11, Annex 11, and global data integrity requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading complex, enterprise-level system implementations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of change control, deviation management, CAPA, and quality systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to influence senior stakeholders and drive cross-functional alignment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PMP or equivalent project management certification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;GAMP, ITIL, or related compliance certification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading CSA transformation initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience related to administration, operation, and maintenance of Laboratory Information Management Systems (LIMS) Chromatography Data Systems, Spectrophotometry Systems, and ancillary/supporting laboratory systems in a GxP environment (Openlab, Cary UV systems, Watson)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pharmaceutical or CRO experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior regulatory inspection leadership experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Risk-based decision making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuous improvement mindset\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$145,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$165,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005291007,"name":"Information Systems \u0026 Informatics","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5134445007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4630782007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5134445007,"updated_at":"2026-05-11T14:56:56-04:00","requisition_id":"859","title":"Senior Manager, Strategic Sourcing ","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-11T14:56:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Sr. Manager, Strategic Sourcing is a member of a team charged with ownership of end-to-end alignment of Arrowhead drug product production. This role oversees the team responsible for strategic sourcing supporting GMP site manufacturing.\u0026amp;nbsp; This person will manage and drive activities related to sourcing, contract management, and supplier management, including the development of sourcing strategies and managing RFx (RFI, RFQ, RFP) processes through award and contracting execution. These responsibilities require cross-functional collaboration with team members from other Technical, Legal, Finance, Quality, and Regulatory functions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead site Sourcing team to ensure sourcing projects are adequately managed to meet project goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coach and mentor team in the creation of personal goals, development, and performance improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate, maintain, and approve training materials, support onboarding of new team members, conduct continuous learning sessions with existing team members and drive engagement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Primary point of contact for supplier escalations within supply base coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with internal stakeholders to manage suppliers, including business requirements, risk management, supplier evaluation and qualification, contracting, and performance management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain sourcing tracking tools (ex. Smartsheet, Excel, Power BI)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Planning team to develop effective supply plan and ensure risk management plan is in place and kept up to date for critical supply\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with Quality on audits, investigations, complaints, change control and GMP systems monitoring, and follow through with action plan implementation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support supplier QMS processes for CAPA/SCAR/DEV/CNs and ASL (Approved Supplier List) accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate supplier risk management program in partnership with internal stakeholders - identification, assessment, mitigation planning and execution including metrics to report on supplier health status and escalating business risks as needed. Including, leading or participating in Business Reviews\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Negotiate and manage contracting required to manage GMP suppliers (e.g. Master Services Agreements, Supply Agreements)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Quality to ensure timely establishment and administration of Quality Agreements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for RFx (RFI, RFQ, RFP) processes and strategic sourcing activities, collaborating with internal stakeholders to support overall business needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage RFx process, including development of requirements, drafting RFx (RFI, RFQ, RFP) documents, facilitating team meetings, and supporting contract negotiations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support internal stakeholders by reviewing all aspects of the sourcing process, including evaluating supplier capabilities and risk identification/mitigation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present business cases and award justifications to leadership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in Supply Chain, Chemistry, Engineering, or related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10 years of increasing responsibility in a pharmaceutical company, contract manufacturing organization or contract research organization including direct report experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5 years of purchasing experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working within an ERP system\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with external vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent negotiating and leadership skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Microsoft Office Suite\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to influence cross-functional change and create/build relationships at all levels of the organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated strength in written and verbal communication, and excellent interpersonal and relationship management skills, with the ability to communicate effectively at all levels of the organization.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proficient using D365\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;APICS/ASCM certifications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to adapt quickly to changing business needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to drive cultural change while improving efficiencies and processes.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$140,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013155007,"name":"Plant Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5131625007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4629262007,"location":{"name":"Pasadena, California, United States"},"metadata":null,"id":5131625007,"updated_at":"2026-06-12T10:58:27-04:00","requisition_id":"856","title":"Senior Payroll \u0026 Benefits Specialist","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-07T16:27:36-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals is seeking a highly motivated Senior Payroll \u0026amp;amp; Benefits Specialist to join our People Services \u0026amp;amp; Culture team. Reporting to the Associate Director of Payroll \u0026amp;amp; Benefits, this role will be responsible for assisting with the end-to-end processing of biweekly payroll and day-to-day benefit support for employees across four locations: Pasadena, CA; San Diego, CA; Madison, WI; and Verona, WI. The Senior Specialist will also process off-cycle payrolls as needed.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In addition, this individual will oversee the administration of daily and quarterly equity compensation transactions, including processing new grants, stock option exercises and restricted stock unit (RSU) activity. Collaboration with the Accounting team and broader People Services \u0026amp;amp; Culture department will be essential to ensure accuracy and compliance.\u0026amp;nbsp; In addition to administration of equity compensation, the Sr Specialist will support the broader People Services \u0026amp;amp; Culture team in general HR related areas.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a full-time, onsite position at Arrowhead’s Corporate Headquarters in Pasadena, CA.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Back up for all payroll activities, including calculating final pay for upcoming terminations and processing their separation through ADP WFN.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Creating and maintaining equity compensation checklists, routing as needed in a timely manner for completion, and closing out checklists once complete.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Key player in managing company’s equity plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help to ensure equity processes comply with federal, state and local regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Backup for reviewing and processing biweekly timecards; following up with employees and supervisors as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain electronic equity filing systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Backup for tracking or managing benefits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct audits as needed to ensure all employee changes and pay data has been entered\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide benefit support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide system support and focus on process improvement on all areas of HR\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support general HR/People Services tasks as needed\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;4 recent years of payroll \u0026amp;amp; benefits experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Associate degree\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to follow verbal and written instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to keep up with a fast past while maintaining attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to gather, analyze and interpret information for completeness and accuracy, and excellent organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recent experience with current version of ADP WFN and advanced Excel skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of wage and hour laws related to payroll.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of equity compensation administration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office suite.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills (oral \u0026amp;amp; written); ability to effectively interact with others at all levels – within and outside of finance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexibility to put in extra hours during critical times.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong time management with the ability to work independently and in a group setting.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelors degree\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$85,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$110,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005290007,"name":"People Services \u0026 Culture","child_ids":[],"parent_id":null}],"offices":[{"id":4005208007,"name":"Pasadena, CA","location":"Pasadena, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5150683007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4638750007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5150683007,"updated_at":"2026-05-29T17:00:08-04:00","requisition_id":"879","title":"Senior Quality Assurance Specialist - External Quality","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-29T17:00:08-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The purpose of this position is to provide quality assurance support to programs utilizing contract development, manufacturing, and testing organizations. The incumbent will review vendor documentation and perform lot disposition per applicable quality agreements as well as capture quality data and generate metrics for vendors. The incumbent will be expected to interact with internal departments as well as multiple contract organizations to support ongoing pre-clinical and clinical development programs at Arrowhead Pharmaceuticals, Inc.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Interact with personnel companywide to obtain the necessary information and details to provide quality assurance support of development, clinical, and commercial programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve vendor generated documentation, including but not limited to, master and executed batch records, testing records, certificates of analysis (CoA), labels, protocols, and reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform lot disposition and generate certificates of compliance (CoC) as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with vendors on quality events and non-conformances as outlined in the applicable quality agreement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and release of completed manufacturing batch documentation including Quality Control data and issuance of Certificates of Analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organization and control of quality, compliance, and project related documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain knowledge of current compliance expectations and regulations pertaining to drug development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with, and provide quality support for, other departments (QC, Project Management, Toxicology, Clinical Operations, Supply Chain, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in meetings with vendors and external organizations as the QA team representative.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties consistent with the position as assigned from time to time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with tracking vendor quality metrics; notify QA management of any performance issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with preparation, update, review, and routing of Arrowhead procedural documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft, review, and approve standard operating procedures (SOP) and work instructions (WI) as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other QA duties as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 8 years of quality assurance or similar experience in a pharmaceutical development company and/or contract manufacturing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of drug GMP regulations, as well as ICH/FDA guidance documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills and ability to communicate with internal and external parties.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated team player willing to contribute to a growing pharmaceutical organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with minimal supervision and as well as manage priorities within a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A detail-oriented self-starter who endeavors to anticipate and resolve problems and seeks opportunities to grow their role and responsibilities at Arrowhead.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience with quality systems supporting drug-device combination products per 21 CFR Part 3 and medical devices QSR per 21 CFR Part 820/ISO 13485 is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office programs, and SmartSheet.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$90,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$110,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5007197007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4571118007,"location":{"name":"Madison, Wisconsin, United States"},"metadata":null,"id":5007197007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"653","title":"Senior Scientist I, DMPK","company_name":"Arrowhead Pharmaceuticals ","first_published":"2025-12-17T17:49:54-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals is seeking an accomplished Senior Scientist, DMPK to play a key role in advancing our growing pipeline of RNAi-based therapeutics. As a senior member of the Drug Metabolism and Pharmacokinetics (DMPK) function, you will partner closely with multidisciplinary teams of chemists, biologists, and translational scientists to shape strategies that enable successful candidate nomination and IND submissions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In this high-impact role, you will lead the design and execution of preclinical DMPK studies, guide interpretation of complex PK/PD data, oversee internal and external study activities, and ensure delivery of high-quality datasets that meet regulatory expectations. The ideal candidate brings deep technical expertise, strong problem-solving skills, and the ability to thrive in a fast-paced, collaborative environment dedicated to scientific excellence and innovative drug development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement in vitro and in vivo DMPK strategies to support preclinical development for compounds across multiple indications and routes of administration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage all DMPK activities, including oversight of internal resources and CRO partners to ensure high-quality and timely data delivery.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design, supervise, and execute preclinical PK studies, including non-compartmental analysis (NCA), data interpretation, reporting, and communication of PK/PD insights to project teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and deliver IND-enabling DMPK packages, ensuring compliance with regulatory expectations and contributing to regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply working knowledge of GLP/GCP principles and ensure appropriate documentation for regulated studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support GLP toxicokinetic (TK) study design, analysis, and reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee metabolite identification in preclinical and clinical samples using high-resolution mass spectrometry (HRMS).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to a dynamic, fast-paced DMPK team by offering scientific leadership, troubleshooting support, and cross-functional collaboration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a current understanding of clinical pharmacology literature and regulatory guidance for oligonucleotide/RNAi therapeutics.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in Pharmacometrics, Drug Metabolism, Pharmaceutical Sciences, or a related discipline with at least 3 years of industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep and broad expertise in DMPK, with working knowledge of nucleotide or oligonucleotide drug metabolism and distribution highly desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with in vitro ADME assays, in vivo PK studies, drug–drug interaction (DDI) evaluations, and Phoenix WinNonlin.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with LC–MS/MS and HRMS, ideally applied to oligonucleotide therapeutics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong background in organic chemistry, biochemistry, and drug biotransformation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience in drug development and understanding of regulatory processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, verbal, and written communication skills, with the ability to interpret and present complex scientific data clearly.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$115,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$140,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005298007,"name":"Clinical Pharmacology \u0026 DMPK","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=4995119007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4565405007,"location":{"name":"Madison, Wisconsin, United States; San Diego, California, United States"},"metadata":null,"id":4995119007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"641","title":"Senior Scientist / Principal Scientist, Clinical Pharmacology","company_name":"Arrowhead Pharmaceuticals ","first_published":"2025-12-01T20:09:39-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role provides clinical pharmacology and pharmacometrics leadership for assigned development programs and may be based in San Diego, CA or Madison, WI. The position is responsible for contributing to clinical trial design, authoring key protocol and regulatory sections, and performing hands-on PK/PD analyses to guide dose selection and program strategy. It oversees the preparation and authorization of PK analysis reports, CSR content, and clinical pharmacology components of global regulatory submissions\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide Clinical Pharmacology and pharmacometrics leadership for designated programs, contribute to design of clinical trial protocols and relevant sections in Investigational Brochure (IB), conduct hands-on analysis of clinical or translational PKPD data, support dosing strategies and clinical pharmacology planning. Authorize clinical PK analysis reports and relevant sections in the Clinical Study Report (CSR).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide high quality documentation of clinical pharmacology analysis compatible with global regulatory submission requirements. Authorize clinical pharmacology modules of CTD to support global filings of marketing application.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide timely communication of analysis results and interpretation with drug development teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a current understanding of clinical pharmacology literature and regulatory guidance for oligonucleotide/RNAi therapeutics\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;PhD or PharmD in the field of pharmacokinetics, pharmacology or pharmaceutical science,\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3 years of pharmaceutical industry experience in clinical-stage drug development.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good understanding of FDA/EMA/ICH guidance related to clinical pharmacology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Established experience in clinical NCA PK analysis and data reporting using Phoenix WinNonlin with familiarity of authorizing PK study report.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in NONMEM and skill of population PKPD modeling is essential.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PBPK/PD modeling\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$120,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$170,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005298007,"name":"Clinical Pharmacology \u0026 DMPK","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null},{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5130592007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4628810007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5130592007,"updated_at":"2026-05-06T14:09:04-04:00","requisition_id":"854","title":"Senior Specialist, Quality Assurance (2nd Shift)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-06T14:07:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The purpose of this position within the Quality Assurance department is to support on-going development programs for preclinical, clinical, and commercial drug candidates at Arrowhead.\u0026amp;nbsp; A key function of the position will involve continued development and maintenance of quality systems supporting Good Manufacturing Practices (GMP) within the organization. The Senior Specialist is expected to interact with multiple internal departments, as well as assist with quality oversight functions for external organizations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;2\u0026lt;sup\u0026gt;nd\u0026lt;/sup\u0026gt; shift work hours are ~1:00 p.m. – 11:30 p.m., Monday – Thursday, includes shift differential\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Review and approval of internal and vendor generated documentation, including master batch records, executed batch records, labels, certificates, reports, and testing records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform QA on the floor and manufacturing room release.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and release of completed manufacturing batch documentation including Quality Control (QC) and Analytical Development (AD) data and issuance of Certificates of Analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Writing, review, change control, approval, issuance, and organization of applicable procedural documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Issuance, review, tracking, and completion of internal quality events (QEs), such as deviations, out of specifications (OOS), and CAPAs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organization and control of quality, compliance, and project related documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain knowledge of current compliance expectations and regulations pertaining to drug development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with, and provide quality support for, other departments (Manufacturing, QC, AD, Project Management, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in meetings as the QA team representative as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Additional duties as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of a bachelor\u0026#39;s degree in a science discipline, or equivalent required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of eight (8) years of experience working in a regulated environment with preference to quality assurance and/or manufacturing experience or equivalent required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills and ability to communicate effectively with internal and external parties.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work with diverse professionals and promote cooperation, shared understanding, and commitment to ensuring best in class quality assurance protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated team player willing to contribute to a growing pharmaceutical organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and manage priorities within a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A detail-oriented self-starter who endeavors to anticipate and resolve problems and seeks opportunities to grow their role and responsibilities at Arrowhead.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of drug GMP regulations, as well as ICH/FDA guidance documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of document control requirements in an FDA regulated organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability for occasional business travel.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with quality systems supporting GMP regulations (21 CFR Parts 11, 210, 211, and EU GMP, including Annex 11 and 15).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competent knowledge of and ability to use Microsoft Word, Excel, and Smartsheet.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with use of an electronic document management system in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$90,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$110,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5076334007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4603800007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5076334007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"790","title":"Specialist III, Quality Assurance (Raw Material Qualification)","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-11T12:36:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The purpose of this position is to provide Quality Assurance support for Arrowhead Pharmaceuticals’ raw materials program. As a member of the Supplier Quality team, this role supports raw material supplier qualification, material risk assessment, specification development, and change control activities to ensure compliance with GMP and applicable regulatory requirements. The position also assists with the collection, analysis, and generation of supplier performance metrics to support ongoing monitoring and continuous improvement. This role requires regular interaction with internal cross-functional stakeholders as well as external organizations to support pre-clinical, clinical, and commercial manufacturing programs\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist with raw material lifecycle management including, but not limited to, drafting, editing, reviewing, and approving raw material specifications, reviewing raw material qualification protocols and reports, and ensuring compliance with periodic requalification cycles, in collaboration with internal functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform risk assessments for raw materials (e.g., impact to product quality, patient safety, and regulatory compliance).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advise Supplier Quality Audits team with supplier qualification and requalification as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support maintenance of the ASL by providing and entering qualification information into the eQMS\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with raw material suppliers to resolve quality issues, documentation discrepancies, and non-conformances per internal procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review Supplier Change Notifications and assess impact on product quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initiate and manage change controls related to raw materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage Supplier Corrective Action Requests (SCARs) per internal procedures and applicable quality agreements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support deviation investigations, CAPAs, and root cause analyses involving material issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide quality oversight during material onboarding and lifecycle management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Request and review supporting documentation for raw material qualifications from suppliers including, but not limited to, production records, certificates of analysis (CoA), certificates of conformance (CoC), BSE/TSE statements, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Scan and upload executed documents to the EDMS, properly categorize within the system, and route for verification/approval.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with the preparation, update, review, and routing of Arrowhead procedural documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track and trend raw material-related quality metrics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with other QA duties as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA in Chemistry, Biology, Biochemistry, or related scientific field is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5+ years of Quality Assurance experience in a GMP-regulated biotech or pharmaceutical manufacturing environment, with an emphasis on raw material release, Supplier Quality, and/or material qualification activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of 21 CFR Parts 210/211, ICH Q7, and applicable global regulatory expectations (e.g., FDA, EMA, Health Canada), along with familiarity with relevant regulatory guidance documents.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with use of an Electronic Document Management System (EDMS) in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with use of an Enterprise Resource Planning (ERP) software in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of ICH Q3, Q8, Q9, Q10, and Q11.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office applications, and SmartSheet.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, verbal, and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to consistently communicate with external parties in a professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to follow company procedures, work instructions, and policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent attention to detail and organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with minimal supervision as well as managing priorities within a face-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$85,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$95,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5144851007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4635867007,"location":{"name":"Verona, Wisconsin, United States"},"metadata":null,"id":5144851007,"updated_at":"2026-05-21T18:49:18-04:00","requisition_id":"870","title":"Specialist III, Supplier Quality","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-05-21T18:49:18-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The purpose of this position is to provide quality assurance support for the Supplier Quality Management program in all aspects of qualification, monitoring, and continuous improvement of suppliers, contract manufacturers (CMOs), contract testing laboratories, and material suppliers. This person will be expected to interact with internal departments as well as multiple contract organizations to support ongoing pre-clinical and clinical development as well as commercial programs at Arrowhead Pharmaceuticals, Inc.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support supplier qualification, requalification, and ongoing monitoring activities for raw material suppliers, CMOs, contract laboratories, packaging vendors, and service providers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with stakeholders and suppliers, as needed, on quality events and non-conformances and issue supplier corrective action requests (SCARs), as outlined in the applicable quality agreements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform quality agreement lifecycle management, including but not limited to, drafting, editing, reviewing, approving, and ensuring compliance with periodic review cycles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and assess supplier change notifications for quality and regulatory impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with supplier risk assessments and ensure documentation is current and compliant.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely and accurate documentation within the Quality Management System (QMS).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in establishing and implementing Supplier KPIs (key performance indicators) and actively contribute to the internal Quality Management Review and external Business Review meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify recurring issues and support continuous improvement initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with preparation, update, review, and routing of Arrowhead procedural documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties consistent with the position as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of quality assurance experience in a biotech or pharmaceutical development, manufacturing, or contract manufacturing organization with an emphasis on Supplier Quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience working in Supplier Quality Management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of 21 CFR Parts 210/211, ICH Q7, and applicable global regulatory expectations (e.g., FDA, EMA, Health Canada), along with familiarity with relevant regulatory guidance documents.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with use of an electronic document management system in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office programs, and Smartsheet.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, verbal, and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to consistently communicate with external parties in a professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to follow company procedures, work instructions, and policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent attention to detail and organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with minimal supervision as well as manage priorities within a face-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$85,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$95,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005286007,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4005212007,"name":"Verona, WI","location":"Verona, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5057387007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4595020007,"location":{"name":"Madison, Wisconsin, United States"},"metadata":null,"id":5057387007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"760","title":"Sr Scientist I, Discovery Analytical Chemistry","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-02-19T18:02:13-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;272\u0026quot; data-end=\u0026quot;664\u0026quot;\u0026gt;Arrowhead Pharmaceuticals is seeking a highly motivated Senior Scientist I\u0026amp;nbsp;to join our Discovery Analytical Chemistry team. In this role, you will play a critical part in advancing our protein and protein conjugate therapeutics by developing and implementing advanced LC-MS analytical strategies that support discovery and early process development activities.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;666\u0026quot; data-end=\u0026quot;1103\u0026quot;\u0026gt;This is an opportunity to contribute at a high scientific level - designing innovative analytical solutions, influencing drug discovery direction, and collaborating cross-functionally to solve complex research challenges. The successful candidate will bring deep technical expertise in protein characterization and quantitation, along with the ability to translate analytical findings into meaningful insights that drive program decisions.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1105\u0026quot; data-end=\u0026quot;1321\u0026quot;\u0026gt;You will serve as both a scientific leader and hands-on contributor, independently developing and optimizing analytical methods while mentoring junior scientists and helping shape analytical strategy within the team.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp; \u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop project and technical strategy within area of expertise\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply advanced scientific principles, theories and concepts to a broad range of research problems and develop innovative solutions for analytical problems related to drug discovery and development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and execute analytical studies to facilitate drug discovery and platform development in various disease areas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently design and initiate development of analytical methods and improvement of existing ones\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a project coordinator for on-going and new analytical method development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently and collaboratively with teams to solve scientific /technical challenges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and validate analytical methods to quantify and characterize drugs and impurities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct sample analysis, analyze data/results, interpret the outcome of experiments and integrate scientific findings to gain further understanding of drug properties or synthetic/purification route\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent team to present research findings to cross-function teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify, propose and lead areas for initiatives /improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Influence and support drug discovery/development directions with scientific findings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Train and mentor junior scientists in the team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in analytical chemistry or close related fields with 2+ years relevant industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong hands-on experience of using LC-MS and HPLC for proteins/protein conjugates characterization and quantitation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in sample preparation, peptide mapping, MS/MS peptide sequencing, glycosylation analysis, disulfide bond mapping, and post-translational modifications analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of protein chemistry and analytical chemistry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiar with routine maintenance of mass spectrometers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong troubleshooting and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent ability for data interpretation and integration\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and presentation skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability and willingness to learn cutting edge technologies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to prioritize the workload and adapt to fast changes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Open mind and willing to learn new technology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with a wide range of analytical techniques\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;hands on experience with CE or MALS is a plus but not necessary\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Wisconsin pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$125,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005284007,"name":"Discovery Chemistry","child_ids":[],"parent_id":null}],"offices":[{"id":4005211007,"name":"Madison, WI","location":"Madison, Wisconsin, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://arrowheadpharma.com/careers/?gh_jid=5091349007","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4610467007,"location":{"name":"San Diego, California, United States"},"metadata":null,"id":5091349007,"updated_at":"2026-04-29T19:14:50-04:00","requisition_id":"817","title":"Sr. Scientist I, Translational Genetics \u0026 Real-World Evidence","company_name":"Arrowhead Pharmaceuticals ","first_published":"2026-03-26T19:16:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI \u0026amp;amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI.\u0026amp;nbsp; Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Position\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Scientist will contribute to the integration of human genetics, multi-omics datasets, and real-world clinical data to generate human evidence supporting therapeutic development. This role will work at the intersection of translational genetics, computational biology, and real-world evidence (RWE) analytics to support target validation, patient stratification, clinical endpoint evaluation, and indication prioritization across Arrowhead therapeutic programs. The successful candidate will collaborate closely with the Translational Genetics \u0026amp;amp; Data Science team as well as cross-functional partners including Real-World Evidence, Clinical Development, Translational Medicine, and Discovery Biology. The role will leverage large-scale biobank datasets, electronic health records (EHR), and other clinical datasets to translate human data into actionable insights supporting drug discovery and development. This position will play an important role in converting Arrowhead’s growing access to biobank data and established computational pipelines into high-value insights that inform therapeutic strategy and precision medicine approaches.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;This role is onsite 5 days a week in San Diego.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Integrate human genetics, multi-omics datasets, and real-world clinical data to generate evidence supporting therapeutic target validation and indication prioritization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze large-scale biobank and population datasets to identify genetic associations and disease mechanisms relevant to Arrowhead therapeutic programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with the Real-World Evidence (RWE) team to analyze clinical datasets including electronic health records (EHR), claims databases, registries, and longitudinal cohort data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct statistical and computational analyses to characterize disease progression, patient heterogeneity, and treatment outcomes using real-world datasets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate genetic findings and clinical observations into hypotheses that inform biomarker strategies, patient stratification, and clinical trial design\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop scalable analytical workflows to integrate genetics, omics, and clinical data sources\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work collaboratively with cross-functional teams including Discovery Biology, Clinical Development, Translational Medicine, and Data Science to support program decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present results to internal stakeholders and contribute to internal reports, project discussions, and scientific publications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage multiple projects simultaneously and communicate progress and findings effectively to project teams and leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to data governance and compliance standards when working with sensitive clinical datasets\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in Biostatistics, Statistical Genetics, Epidemiology, Bioinformatics, Computational Biology, Biomedical Data Science, or a related quantitative discipline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in human genetics, biomedical data science, or real-world data analytics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience leveraging AI/LLMs to accelerate end-to-end research workflows, including coding, data analysis, literature synthesis, and report generation, with demonstrated improvements in efficiency and output quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with biobank-scale datasets and real-world data sources such as EHR, claims databases, registries, or population cohorts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong background in statistical genetics, epidemiology, or observational data analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience integrating genetics, omics, and clinical datasets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in R or Python for large-scale data analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent problem-solving, analytical, and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work effectively in a fast-paced, collaborative, and cross-functional research environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Post-doc and industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience analyzing large-scale population genetics datasets such as UK Biobank, FinnGen, All of Us, or Genomics England\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with analytical frameworks including phenome-wide association studies (PheWAS), Mendelian randomization, causal inference methods, and survival analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with real-world clinical data models such as OMOP / OHDSI\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience collaborating with clinical development or real-world evidence teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience applying machine learning or advanced statistical methods to biomedical datasets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interest in translating human data into actionable insights for drug development\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California pay range \u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$145,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$165,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Arrowhead provides competitive salaries and an excellent benefit package.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Candidates must have current, valid authorization to work in the country where this role is located.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;a href=\u0026quot;https://arrowheadpharma.com/wp-content/uploads/2023/09/Arrowhead-California-Applicant-Privacy-Policy.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;California Applicant Privacy Policy\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005285007,"name":"Biology","child_ids":[],"parent_id":null}],"offices":[{"id":4005210007,"name":"San Diego, CA","location":"San Diego, California, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":69}}