{"jobs":[{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5017289008?gh_jid=5017289008","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":4379201008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5017289008,"updated_at":"2026-03-09T18:31:21-04:00","requisition_id":"T14-830-2025","title":"AI Implementation Consultant – Legal ","company_name":"Vaxcyte","first_published":"2025-12-02T23:09:53-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte’s Legal team is seeking a motivated, forward-thinking AI Consultant to support the design, evaluation, and implementation of emerging AI solutions across Legal and Compliance functions. This project-based role is ideal for a student pursuing their MS or PhD with strong technical skills, curiosity about legal operations, and a passion for applying AI to real-world business problems. You will work closely with cross-functional teams to prototype, test, and deploy AI tools that drive efficiency, enhance compliance workflows, and expand the team’s ability to deliver strategic support to the business.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bot Development: Design and prototype an AI-powered chatbot to support Legal and Compliance functions (e.g., FAQs, SOP references, or workflow routing).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Legal Dashboard Enhancements: Enhance the existing Legal Dashboard using Box AI and related integrations to improve automation, visibility, and user experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tool Evaluation: Research, evaluate, and recommend emerging AI tools and products; schedule and participate in demos; provide post-demo analysis and recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implementation Support: Assist with tool rollout, user onboarding, and training materials for Legal, Compliance, and other stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuous Exploration: Identify and scope new AI use cases within Legal and related functions, collaborating with IT and Operations as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;AI Tool Integration: Support implementation and optimization of existing Legal AI tools such as Spellbook and CoCounsel to ensure full functionality and adoption across teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;System Connectivity: Collaborate with IT to integrate and connect AI tools and software applications, enabling seamless read-only and action-based access across platforms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Enrolled in an MS or PhD program pursuing a degree in Computer Science, Data Science, Engineering, AI or a related field.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of generative AI concepts (e.g., open-source small LLMs, MCPRAG and API integrations).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and analytical skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to translate technical concepts into practical applications for non-technical teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using or configuring AI tools such as Box AI, Microsoft Copilot, ChatGPT Enterprise, or similar platforms is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior exposure to automation tools or workflow design (e.g., Power Automate, Zapier, or custom bots) is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated project management or client-facing experience (internships count!) is preferred.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Sr. VP, General Counsel, Chief Compliance Officer \u0026amp;amp; Corporate Secretary\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos; Open to Remote\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12-months (this is a part -time role that is project based)\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range: \u0026lt;/strong\u0026gt;$40.00 - $50.00 per hour\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;(SF Bay Area). Hourly ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5236266008?gh_jid=5236266008","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":4482468008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Remote","value_type":"single_select"}],"id":5236266008,"updated_at":"2026-06-04T11:48:18-04:00","requisition_id":"655-515-2026","title":"Associate Director, CMC Statistician","company_name":"Vaxcyte","first_published":"2026-06-04T11:48:18-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for an energetic and talented individual to join Vaxcyte\u0026#39;s Global Analytical organization as Associate Director, CMC Statistician. The position will be an integral part of the Vaccine Specification Working Group (VSWG), providing statistical leadership for specification setting and Justification of Specifications (JOS) across late-stage development, PPQ, BLA readiness, and commercial lifecycle management. This individual will collaborate with Process Development, MSAT, Stability, Quality, Regulatory Affairs, Manufacturing, and external partners to develop statistically sound, patient-centric, and regulatory-ready approaches. The ideal candidate will bring deep CMC statistics experience in biotech/pharma, excellent technical writing and communication skills, and a practical, data-driven approach to cross-functional decision making.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Functions:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the CMC statistical lead for the VSWG, supporting specification-setting strategy for drug substance, drug product, intermediates, raw materials, release testing, stability testing, and in-process testing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop statistical strategies for specification and JOS using clinical experience, manufacturing experience, stability behavior, analytical variability, assay capability, and process capability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and execute statistical analyses such as confidence intervals, prediction intervals, tolerance intervals, regression, ANOVA, DOE, equivalence testing, trend analysis, control charts, and Cpk/process capability analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide statistical input to late-stage development, PPQ, BLA/MAA preparation, health authority responses, commercial readiness, and specification lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review statistical sections of specification and JOS documents, CMC technical reports, regulatory submission sections, and briefing materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess analytical method performance and method lifecycle changes, including precision, transfer/bridging, comparability, and impact of analytical variability on specification decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Process Development, MSAT, Stability, QA, RA, Manufacturing, and external partners to align statistical rationale with CMC control strategy and regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support PPQ, APR, and CPV activities by evaluating process consistency, state of control, trends, internal control limits, and capability relative to proposed or registered specifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate complex statistical concepts into clear recommendations for cross-functional teams, senior leaders, and non-statistical stakeholders; support audits, inspections, and health authority interactions 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;p\u0026gt;MS or PhD in Statistics, Biostatistics, Applied Statistics, Mathematics, Data Science, or a related quantitative discipline with 10+ years of experience in the pharmaceutical or biotechnology industry. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Significant hands-on experience in CMC statistics, including specification setting, JOS preparation, analytical method evaluation, stability analysis, process validation, PPQ, CPV, and/or commercial manufacturing support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience supporting BLA, MAA, IND, or major health authority submissions and responses; BLA experience strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of late-stage and commercial specification-setting principles, including clinical relevance, patient-centric justification, manufacturing experience, analytical capability, stability data, and lifecycle considerations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with vaccines, biologics, complex modalities, multivalent products, conjugates, or adjuvanted products is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong expertise in statistical methods used in CMC and analytical development, including regression, ANOVA, DOE, equivalence testing, tolerance/prediction intervals, control charts, process capability, and stability/shelf-life modeling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with statistical software such as R, SAS, JMP, Python, Minitab, or equivalent tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive understanding of relevant regulatory expectations and guidance, including FDA, EU, WHO, and ICH principles applicable to biologics/vaccines, specifications, analytical methods, validation, stability, and lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant experience authoring technical and regulatory-ready documents, including statistical reports, JOS sections, protocols, validation reports, SOPs, and CMC submission content.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills, both written and verbal; able to explain complex statistical concepts clearly and influence cross-functional decisions in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic and analytical decision-making skills; able to navigate ambiguity, prioritize across competing demands, and implement practical, phase-appropriate, and compliant approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-starter with proven project management capability and the ability to work independently in a remote, matrixed, and highly collaborative environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt; Senior Director, Global Analytical Lead - Commercial Readiness and Analytical Strategy\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; San Carlos, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Remote\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt; $170,000 - $198,000\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043044008,"name":"Analytical","child_ids":[],"parent_id":4043043008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/4974572008?gh_jid=4974572008","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":4362180008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Remote","value_type":"single_select"}],"id":4974572008,"updated_at":"2026-06-05T19:35:50-04:00","requisition_id":"610-320-2025","title":"Associate Director, Global Drug Substance Commercialization, Critical Raw Materials","company_name":"Vaxcyte","first_published":"2025-11-07T14:40:54-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director for Drug Substance (DS) Commercialization has the accountability for launch readiness and commercial supply of associated raw materials for production of eCRM and associated components for glycoconjugate vaccines. This role focuses on technical launch planning and execution by bringing best-practices and coordinating cross-functional efforts for regulatory filings, and commercial supply of associated raw materials for production of eCRM and associated components for glycoconjugate vaccines and post-launch process robustness initiatives.\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;This role also provides leadership to ensure that the organization is equipped to effectively communicate the scientific and commercial rationale for eCRM and associated raw material processes to internal stakeholders, relevant CMOs, and to regulatory agencies. The incumbent will work with the organization to ensure on-time execution and appropriate planning for commercial lifecycle management.\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;This position will be reporting into the Senior Director for Global DS Commercialization, Protein. The Associate Director will collaborate on overall program strategy, with primary responsibility for supporting development and execution of eCRM and associated raw material process strategy execution, including process troubleshooting, robustness study design and execution. \u0026amp;nbsp;The incumbent will also contribute to authoring of regulatory documentation and associated supporting documents. \u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;Global Manufacturing Science and Technology (GMSAT) is responsible for successfully and seamlessly transitioning the vaccine process from Process Development to Commercial, developing and executing technical launch and commercialization strategy, continuously improving process robustness through to end of lifecycle, and ensuring best possible patient outcomes while creating value for the enterprise. As part of the Technical Operations organization, GMSAT will lead the technical and process support for end-to-end commercial manufacturing, including Polysaccharides, Carrier Proteins, Conjugation across all Drug Substances (DS). The range of activities will include DS technology transfer support, process characterization experiments in support of validation, process improvement, evaluation of novel process technologies, and investigation of process related manufacturing issues, ensuring continuous improvement in process robustness throughout the product life cycle etc. \u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;DS Commercialization – \u0026lt;/strong\u0026gt;Provide strategic and scientific leadership for eCRM and associated raw materials with internal and external stakeholders and ensure successful execution of launch plans and post-launch commercial activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Process robustness\u0026lt;/strong\u0026gt; – Continuously improve process understanding and process robustness by putting systems in place to monitor, trend, and optimize operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Interface\u0026lt;/strong\u0026gt; - Collaboration with cross-functional teams across the network, including Regulatory, Process Development, Quality, Supply Chain, Procurement, and DS Operations, to drive the successful development and commercial launch of carrier proteins for pipeline products. Provides technical representation into initial technology transfer, product launch, product lifecycle, to the end of life/product retirement and for defining/developing the next generation of production technologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Tech-transfer new technologies\u0026lt;/strong\u0026gt; - Ensure robust processes exist to support technical transfers and integration of new technologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Support\u0026lt;/strong\u0026gt; \u0026lt;strong\u0026gt;technical services\u0026lt;/strong\u0026gt; - Support of our internal and external manufacturing network, including materials management and data analytics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Process validation and comparability\u0026lt;/strong\u0026gt; - Provide support for the execution of process validation and process comparability activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Regulatory\u0026lt;/strong\u0026gt; - Engage In technical authoring and reviewing of regulatory filings and responding to questions received from health authorities. Effectively communicate the scientific and commercial rationale for DS processes to the Boards of Health for regulatory submissions for commercialization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Communicate\u0026lt;/strong\u0026gt; - Effectively and efficiently communicate process performance to key stakeholders (internal-facing and external-facing). Connect and build strong working relationships with others, demonstrating strong emotional intelligence and an ability to communicate clearly and persuasively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Executing for Results - \u0026lt;/strong\u0026gt;Set clear and challenging goals and take accountability for driving results. Comfortable with ambiguity and uncertainty; the ability to adapt nimbly and lead others through complex situations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Leadership\u0026lt;/strong\u0026gt; - Contribute as member of the DS Commercial MSAT team, with an aim to ensure effective and efficient delivery of our life-enhancing therapies to our patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Travel\u0026lt;/strong\u0026gt; 10-20% travel required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Degree(s) in Chemical or Biochemical Engineering, Chemistry, Biochemistry, or related discipline with a minimum of 9+ years of relevant experience for Ph.D., 11+ years for M.S./M.A., or 14+ years for B.S./B.A.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Broad experience in protein processes, including bacterial fermentation, recovery, and purification across multiple operational scales. \u0026amp;nbsp;Experience with pneumococcal conjugate vaccines strongly desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leadership experience in MSAT or Process Development in supervisory and/or matrixed team roles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to leverage deep technical knowledge in a collaborative manner to achieve collective goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organization, problem solving and strategic planning skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly skilled in both verbal and written communication with the ability to interact effectively with people of diverse backgrounds and perspectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively recognizes needs and potential challenges, and independently identifies and implements effective steps and solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The ability to seek and analyze data from a variety of sources to support decisions and to align others with the organization\u0026#39;s overall strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An entrepreneurial and creative approach to developing new, innovative ideas that will stretch the organization and push the boundaries within the industry.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Director, Global Drug Substance Commercialization Lead, Protein\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;Open to Remote, prefer San Carlos, CA or Raleigh, NC\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Remote\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$174,000 - $203,000\u0026amp;nbsp;(SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4046550008,"name":"Global MSAT","child_ids":[],"parent_id":4043054008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5173193008?gh_jid=5173193008","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":4452917008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Remote","value_type":"single_select"}],"id":5173193008,"updated_at":"2026-05-01T19:57:01-04:00","requisition_id":"740-320-B","title":"Associate Director, Process Validation and Risk Management","company_name":"Vaxcyte","first_published":"2026-04-02T22:16:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Process Validation and Risk Management will lead and facilitate commercial process validation and risk management activities across Vaxcyte’s end-to-end manufacturing processes. This role focuses on technical strategy, execution, and cross-functional coordination to support commercial readiness, regulatory compliance, and lifecycle management.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The incumbent will provide leadership to ensure the organization is equipped to effectively design, execute, and communicate process validation and risk management strategies to internal stakeholders, external partners, and regulatory agencies.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position will report to the Sr. Director of Process Validation within the Global MSAT organization and will collaborate on overall validation strategy, with primary responsibility for process validation execution and risk management frameworks supporting commercial manufacturing.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Process Validation Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic and scientific leadership for process validation (PPQ, CPV, lifecycle validation) across commercial programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and facilitate execution of validation strategies to support technology transfer, site readiness, and product launch.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment of validation activities with regulatory expectations and lifecycle management plans.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Risk Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement risk management frameworks, tools, and processes in collaboration with Quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead cross-functional risk assessments to identify, evaluate, and mitigate operational, technical, and regulatory risks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and communicate risk trends and key risk indicators to stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Commercialization \u0026amp;amp; Lifecycle Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support commercial manufacturing operations by ensuring processes remain in a validated and controlled state.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to lifecycle management activities, including process improvements and continued process verification.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Cross-functional Interface\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Regulatory, CMC, Quality, Supply Chain, Procurement, and Engineering to support commercialization and supply continuity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with internal teams and external CMOs to ensure alignment on validation and risk strategies.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Technical Oversight\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance for validation of processes, systems, facilities, and methods within the commercial organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support deviation investigations, ensuring timely resolution and sustained compliance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Regulatory\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to authoring and reviewing regulatory filings and responses to health authorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively communicate the scientific and commercial rationale for validation and risk management strategies.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Process Validation \u0026amp;amp; Comparability\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership for execution of process validation and comparability\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;activities, ensuring data integrity and compliance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Raw Material \u0026amp;amp; Network Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance on raw material qualification strategies to ensure supply reliability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support validation activities across internal and external manufacturing networks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Communication \u0026amp;amp; Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Communicate process validation performance and risk insights to key stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build strong working relationships and influence across a matrixed organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute as a key member of the Global MSAT organization to enable successful commercialization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel - 10-30% domestic and international travel required.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Degree(s) in Chemical or Biochemical Engineering, Chemistry, Biochemistry, or related discipline with a minimum of 9+ years of relevant experience for Ph.D., 11+ years for M.S./M.A., or 14+ years for B.S./B.A.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience in biologics/vaccine manufacturing, including:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Process validation (PPQ/CPV)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;MSAT, technical operations, or late-stage development\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Technology transfer and commercialization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in quality risk management (ICH Q9) and regulatory expectations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated leadership in matrixed or cross-functional team environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to apply deep technical knowledge to develop strategies and drive execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving, organizational, and strategic planning skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and stakeholder engagement skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to analyze data and align stakeholders with organizational strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Innovative and entrepreneurial mindset to drive continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An entrepreneurial and creative approach to developing new, innovative ideas that will stretch the organization and push the boundaries within the industry.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Reports to\u0026lt;/strong\u0026gt;: Senior Director, Process Validation\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; San Carlos, CA or North Carolina\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt; $174,000 – $203,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4046550008,"name":"Global MSAT","child_ids":[],"parent_id":4043054008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5196126008?gh_jid=5196126008","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":4463199008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5196126008,"updated_at":"2026-05-18T13:18:13-04:00","requisition_id":"584-710-2026","title":"Associate Director, Regulatory CMC","company_name":"Vaxcyte","first_published":"2026-04-27T15:09:47-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A hands-on role providing both strategic and operational activities. This role develops and executes multi-product global regulatory CMC strategies for investigational products and leads the preparation and filing of regulatory CMC submissions. Manages interactions with Health Authorities for CMC topics. Provides regulatory CMC guidance to various cross-functional teams and ensures all applicable global regulatory requirements are considered and incorporated into product development. Conducts routine regulatory surveillance and communicates new/changing regulations. \u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Functions:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leads the preparation and review of CMC sections of global regulatory submissions, as well as the interactions and responses with regulatory agencies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Member of technical development teams which require experienced interpretation of applicable EMA/FDA/ICH/Global regulations to ensure CMC compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Defines CMC content (data and documentation) requirements for regulatory submissions and compiles/reviews this content for conformance with established requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides CMC regulatory guidance to cross-functional teams and key stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages regulatory assessment and guidance on product compliance topics including change controls, deviations, and GMP investigations throughout development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads projects with cross-functional teams and acts as the primary regulatory CMC contact for assigned products and projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represents company in Health Authority meetings and leads or supports CMC preparation activities for meetings with Health Authorities on CMC related matters\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stays abreast of current and evolving regulatory CMC requirements, applies this knowledge to assigned projects, and shares knowledge and experience with others to support their development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates in the design, development and implementation of department strategies, providing recommendations in area of expertise\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Bachelor’s Degree in a scientific discipline (e.g. Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices). Minimum 10 years of experience working in vaccine or biotech industry, or in a related field, or the equivalent combination of education and experience. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prior experience preparing/authoring CMC DS sections:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BLA highly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Post-approval supplements/variations highly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;INDs/IMPDs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Prior development or manufacturing experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Computer software skills (LIMS, SAP, TrackWise, Veeva will be used).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal skills to communicate difficult concepts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and strong problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborates and communicates in an open, clear, complete, timely, and consistent manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong sense of planning and prioritization, and the ability to work with all levels of management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced knowledge in regulatory (FDA, EMA, Health Canada and ICH) guidelines\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Executive Director, CMC Regulatory\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA / US Remote\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Remote\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$180,000 - $210,500 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043052008,"name":"Regulatory","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5126186008?gh_jid=5126186008","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":4430829008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5126186008,"updated_at":"2026-05-01T16:29:14-04:00","requisition_id":"702-820-B","title":"Associate Director, SEC Reporting \u0026 Technical Accounting","company_name":"Vaxcyte","first_published":"2026-02-26T14:44:18-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, SEC Reporting \u0026amp;amp; Technical Accounting will serve as a key contributor to the company’s external reporting and technical accounting function. Reporting to the Senior Director, Technical Accounting \u0026amp;amp; SEC Reporting, this role will be highly hands-on, owning the preparation and execution of SEC filings and technical accounting analyses while also managing one direct report.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is ideal for a technically strong accounting professional who enjoys\u0026amp;nbsp;operating\u0026amp;nbsp;in the details, partnering cross-functionally, and helping build processes in a growing public biotechnology company.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;SEC Reporting (Hands-On Execution)\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own the preparation of quarterly and annual SEC filings, including Forms 10-Q, 10-K, and 8-K\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare\u0026amp;nbsp;and/or review\u0026amp;nbsp;primary financial statements, footnotes, and related disclosures\u0026amp;nbsp;in accordance with\u0026amp;nbsp;U.S. GAAP and SEC requirements\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft and support MD\u0026amp;amp;A disclosures, with emphasis on R\u0026amp;amp;D, G\u0026amp;amp;A, stock-based compensation, and other pre-revenue biotech-specific areas\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate the quarterly close-to-reporting process across Accounting, FP\u0026amp;amp;A, Legal, and external auditors\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support earnings release tie-outs and disclosure controls\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Technical Accounting\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support technical accounting assessments and documentation for complex transactions, including:\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaboration, licensing, and R\u0026amp;amp;D-related arrangements\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Equity and equity-linked financing transactions\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other complex\u0026amp;nbsp;and other non-routine transactions\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Research new accounting standards and SEC guidance; assess applicability and implementation impact\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft clear, well-supported technical accounting memos and communicate conclusions to stakeholders\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;Strong experience in ASC 842, including the identification, classification, and accounting of lease arrangements, as well as the preparation and review of related disclosures in compliance with U.S. GAAP\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;People Management\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage and mentor one direct report, providing coaching, review, and development support\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review work products to ensure accuracy, quality, and adherence to timelines\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster strong execution discipline and continuous improvement within the reporting function\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Process Improvement \u0026amp;amp; Scaling\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Help design and enhance scalable SEC reporting and technical accounting processes as the company grows\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with cross-functional teams to ensure accounting and reporting considerations are incorporated into business decisions\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support SOX and internal control documentation\u0026amp;nbsp;related to SEC reporting and technical accounting\u0026amp;nbsp;as applicable\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Bachelor’s degree in Accounting\u0026amp;nbsp;or related field; CPA\u0026amp;nbsp;strongly\u0026amp;nbsp;preferred with a minimum 10 years of progressive accounting experience, including:\u0026amp;nbsp;Public accounting experience (Big 4 or national firm strongly preferred)\u0026amp;nbsp;and/or direct SEC reporting experience at a public company.\u0026amp;nbsp; Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong technical knowledge of U.S. GAAP and SEC reporting requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly detail-oriented with strong execution skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable operating in a fast-paced, evolving environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong ownership mindset with the ability to balance deadlines and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative, proactive, and solutions-oriented\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Ability to work onsite 3 days per week required; and more often based on business needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$184,000 - $215,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043031008,"name":"Accounting \u0026 Finance","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5206550008?gh_jid=5206550008","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":4467944008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5206550008,"updated_at":"2026-05-06T14:00:23-04:00","requisition_id":"T38-535-2026","title":"Associate Engineer II (Contract), Drug Product Process Development","company_name":"Vaxcyte","first_published":"2026-05-06T13:32:41-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking an energetic and talented individual to join the Drug Product (DP) Process Development team within the broader Process Development organization. The primary responsibility of the incumbent will be to provide technical and engineering support across DP process development activities, spanning late-stage clinical supply, process characterization, tech transfer, and commercial readiness (PPQ) of Vaxcyte’s lead programs. The role requires close collaboration with internal cross-functional partners (Formulation, Analytical Development, MSAT, Quality) as well as external contract development and manufacturing organizations (CDMOs) supporting Vaxcyte’s fill/finish operations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Due to the high number of Drug Substances (up to 31) within the DP and the aluminum-containing adjuvant system, this is arguably one of the most complex Drug Products in clinical and commercial development today, offering the right candidate an incredible opportunity to make a significant impact on the product, the company, and the industry. The successful candidate will be hands-on, detail-oriented, and comfortable operating in a fast-paced environment with fluid priorities. The role is predominantly lab- and office-based at Vaxcyte’s San Carlos headquarters, with opportunities to contribute to studies executed at both internal and external (CDMO) sites.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Functions:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Support the development, characterization, and qualification of robust Drug Product processes for late-stage clinical and commercial manufacturing.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Execute bench- and pilot-scale process development studies using down-scaled models, including compounding/mixing, sterile filtration (filter selection and sizing), fill/finish, hold time, and container/closure evaluations.\u0026amp;nbsp;\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Perform in-process sample testing and analysis of DP intermediates and finished product to support process monitoring, process characterization, and release.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Maintain accurate and timely data entry and documentation in Benchling (ELN) in accordance with Good Documentation Practices (GDP), ensuring accuracy, completeness, and compliance with established standards and regulatory requirements.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Analyze experimental and manufacturing data using statistical tools (e.g., JMP), identify trends, and summarize findings in technical reports and presentations.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Perform routine lab upkeep and housekeeping to ensure laboratory cleanliness standards are met and conduct regular inventory monitoring and reconciliation.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Work within a team environment and provide support as necessary to further the team’s initiatives.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;BS in Chemical Engineering, Biochemistry, or a related discipline, with minimum 2 years of relevant industry experience. MS without experience; or equivalent work experience.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Experience in, or exposure to, early- and/or late-stage clinical fill/finish manufacturing under GMP regulations preferred.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Working knowledge of Drug Product unit operations, such as compounding/mixing, sterile filtration, aseptic fill, and container/closure systems (vials, PFS, cartridges).\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Experience supporting technology transfer, scale-up/scale-down, process characterization, or CDMO-based manufacturing activities is preferred.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Familiarity with statistical analysis tools (e.g., JMP, Minitab) is preferred.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Experience using electronic lab notebook (ELN) systems, preferably Benchling, is a plus.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Strong interpersonal and communication skills, both verbal and written, with the ability to work effectively with internal cross-functional teams.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Ability to work independently and collaboratively in a fast-paced, cross-functional environment, managing multiple priorities simultaneously.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Ability to execute, document, and interpret drug product process development and characterization experiments, adhering to scientifically sound practices.\u0026lt;br\u0026gt;• \u0026amp;nbsp; \u0026amp;nbsp;Strong technical writing, data analysis, and communication skills.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Engineer I, Drug Product Process Development\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026lt;/strong\u0026gt; 12 months\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026lt;/strong\u0026gt; 51/hr. – 56/hr.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5168436008?gh_jid=5168436008","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":4450619008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5168436008,"updated_at":"2026-04-15T17:39:25-04:00","requisition_id":"T26-525-2026","title":"Associate Engineer II (Contract), Polysaccharide Manufacturing ","company_name":"Vaxcyte","first_published":"2026-03-27T16:22:07-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Development organization is comprised of four Process teams: Protein, Polysaccharide, Conjugate Drug Substance (Conjugation), and Drug Product. These Process Development teams are supported by Analytical Development and Formulation Development teams. Vaxcyte is seeking an Associate Engineer II with experience or strong foundational knowledge in vaccine or biologics process development and manufacturing to join the Polysaccharide Clinical Manufacturing/Process Development team.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The candidate will provide technical support for manufacturing activities in collaboration with CDMO partners, while also contributing to process development and process validation efforts. The position requires laboratory presence (\u0026amp;gt;50%) and the ability to independently execute and document experiments, analyze data, and communicate results through technical reports and presentations. The successful candidate will collaborate cross-functionally and may interface with external CDMO partners to support manufacturing campaigns and process transfers.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide remote manufacturing (MFG) oversight to support batch execution, ensuring adherence to process parameters and GMP requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in deviation investigations, root cause analysis, and implementation of corrective and preventive actions (CAPAs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical support for MFG and process development through data analysis, MFG document reviews, and supporting lab scale studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform in-process sample testing to support monitoring of MFG process performance and understanding\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage sample inventory, including tracking, storage, and organization of manufacturing samples\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate and timely documentation in electronic lab notebook (ELN) systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze manufacturing and experimental data using statistical tools (e.g., JMP) and summarize findings in technical reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams including Process Development, Manufacturing, Analytical Development, and Quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present technical data to internal stakeholders and support interactions with CDMO partners\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Chemical Engineering, Biochemistry, or a related discipline, with minimum 2 years of relevant industry experience. MS without experience; or equivalent work experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience or exposure to GMP manufacturing environments and process development activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with in-process analytical techniques, including colorimetric and enzymatic assays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with upstream and downstream processing technologies, such as fermentation, UF/DF, depth filtration, and chromatography\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting technology transfer, scale-up, or CDMO-based manufacturing is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of deviation investigations and root cause analysis methodologies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with statistical analysis tools (e.g., JMP) is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using electronic lab notebook (ELN) systems is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong technical writing, data analysis, and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Engineer, MSAT Polysaccharide\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$51.00/hr. - $56.00/hr.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5218340008?gh_jid=5218340008","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":4473977008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5218340008,"updated_at":"2026-05-19T13:07:25-04:00","requisition_id":"T39-535-2026","title":"Associate Scientist I (Contract), Formulation Development ","company_name":"Vaxcyte","first_published":"2026-05-13T11:25:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte has an exciting opportunity for an energetic and talented individual to join our Formulation Development team. The Associate Scientist will play a key supporting role in the development of innovative protein–polysaccharide conjugate vaccines.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful candidate will support formulation development activities to advance Vaxcyte’s drug product pipeline from early development through commercialization. This role will also involve supporting scientists in the execution of experimental studies, as well as the testing and characterization of formulations, supporting investigations, and contributing to process optimization and technical problem-solving.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support for the manufacture of complex drug product formulations for use in analytical and process development, validation of assays etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize the formulation development lab benches and storage space by setting up weekly cleanup schedules with the team, fridge space management, and maintaining the lab to meet safety standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the scientist in execution of experiments by utilizing biochemical, biophysical and particle techniques, and as well as assisting with data interpretation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare buffers and lab reagents for use in manufacturing and testing activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute experiments with scientific rigor and excellent documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position reports into the Formulation Development line\u0026amp;nbsp;and is part of the broader Process Development and Manufacturing group.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant partnerships with the Analytical, Device, and Process Engineering teams will occur; thus, the ability to work within this collaborative environment is essential.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This role requires agility in both thought processes and practical execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In addition, being scientifically pro-active within the small group will be encouraged.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is a lab-based position and requires the ability to stand or sit for extended periods as well as work in biosafety cabinets.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Chemistry, Analytical Chemistry preferred, Organic / Biochemistry considered, with 1-2 years of relevant industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of analytical chemistry or biochemistry principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in calculating buffer recipes and preparing buffers and laboratory reagents is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates highly efficient, organized, and methodical work practices encompassing practical lab tasks, notebook maintenance, and comprehensive record keeping. Prior experience with an Electronic Lab Notebook (ELN) system is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with method troubleshooting and data analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Microsoft Office software (Word, Excel, PowerPoint) is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An understanding of analytical statistical analysis is also preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with GraphPad Prism and JMP is also desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and excellent skills in pipetting and sample preparation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work collaboratively in a cross-functional team environment on multiple projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills, with excellent written and verbal communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Scientist II, Formulation Development\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement:\u0026lt;/strong\u0026gt; Onsite (minimum of 4 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12months\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$40/hr. - $45/hr.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5135307008?gh_jid=5135307008","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":4435001008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5135307008,"updated_at":"2026-05-22T14:22:32-04:00","requisition_id":"630-515-2026","title":"Associate Scientist II, Analytical Development","company_name":"Vaxcyte","first_published":"2026-03-02T17:44:59-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for an energetic and talented individual to join our analytical development team. The primary responsibilities for the successful candidate will include method development, sample testing, analyzing data, and authorizing protocols and reports.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist in analytical method development of new assays.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform analytical testing, data analysis and present in team meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain thorough and accurate records of laboratory work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support daily lab operations, sample inventory and sample shipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author analytical documents including but not limited to test method, protocols, and reports.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Chemistry, Analytical Chemistry preferred, Organic / Biochemistry considered, with 2+ years of relevant industry experience, or MS with 1+ years of experience. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in chemical and biological assays such as colorimetric/ fluorometric microplate assays, PCR/qPCR, HPLC, CE, UV-Vis, ELISA and LC-MS.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of basic principles of analytical method development/ validation/ qualification concepts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and excellent skills in record keeping/documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills and ability to communicate effectively both verbally and in written formats.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position is a lab-based role and requires onsite presence.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;\u0026lt;span class=\u0026quot;cf0\u0026quot;\u0026gt;Senior Scientist, Analytical Development\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Onsite (5 days per week)\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$105,000 – $123,000\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043044008,"name":"Analytical","child_ids":[],"parent_id":4043043008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5191286008?gh_jid=5191286008","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":4460853008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5191286008,"updated_at":"2026-05-18T20:26:23-04:00","requisition_id":"T37-515-2026","title":"Associate Scientist II (Contract), Analytical Development for Characterization ","company_name":"Vaxcyte","first_published":"2026-05-18T20:26:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly skilled and motivated Associate Scientist II (Contract) to join our Analytical Development team to support the characterization of drug substances, protein intermediates, and drug products using LC-MS and complementary analytical techniques The ideal candidate would be central to implementing mass spectrometry-based workflows, interpreting complex data, and collaborating cross-functionally to advance our vaccine programs.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prepare samples and perform analyses per SOPs, including detailed data interpretation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently execute analytical assignments with accuracy and efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement LC-MS workflows for proteins, conjugates, and other in-process molecules.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operate, maintain, and troubleshoot Orbitrap, qTOF, and triple quadrupole mass spectrometers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct rigorous data analysis, interpret results, and present findings in team meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally to develop analytical strategies and support their needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate documentation in an electronic lab notebook system.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Chemistry, Analytical Chemistry, Biochemistry, or a related discipline, with minimum 2 years of relevant industry experience. MS without experience; or equivalent work experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience utilizing mass spectrometry platforms, including hybrid Orbitraps, qTOFs, and triple quadrupoles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiar with peptide mapping, and intact protein analysis workflows.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills, attention to detail, and documentation expertise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific curiosity and problem-solving abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communication and collaboration within cross-functional environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to rapidly learn analytical workflows and technologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using electronic lab notebook (ELN) systems is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Scientific creativity and curiosity for applying new technologies to complex analytical challenges.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Scientist II, Analytical Development\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12 months\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$51/hr. - $56/hr.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5202466008?gh_jid=5202466008","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":4466084008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5202466008,"updated_at":"2026-06-05T19:06:08-04:00","requisition_id":"T28-530-2026","title":"Associate Scientist II (Contract), Conjugation Development","company_name":"Vaxcyte","first_published":"2026-05-06T15:48:52-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking an Associate Scientist II (Contract), Conjugation Development, who will contribute to the development of a robust process for generating the company’s proprietary pneumococcal conjugate vaccine. This role will focus on the synthesis, purification, and analytical characterization of chemically modified polysaccharides and polysaccharide-protein conjugates. The successful candidate will apply a strong foundation in analytical chemistry and laboratory techniques to optimize and troubleshoot processes, while also supporting related areas such as analytical development and stability studies. This position requires strong organizational skills, clear communication, and the ability to work in a fast-paced, cross-functional environment.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform and optimize multi-step syntheses of protein-polysaccharide conjugates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Purify polysaccharides and conjugates using methods including dialysis, size-exclusion chromatography, and tangential flow filtration (TFF).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze polysaccharides and conjugates using methods such as colorimetric assays, HPLC assays, SEC-MALS, and SDS-PAGE, and contribute to method bridging studies and qualification to ensure robustness and consistency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate, well-organized experimental records and support data verification and analysis to enable process optimization and reproducibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with troubleshooting of synthesis, purification, and analytical procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track inventory of critical reagents and assist with ordering as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support maintenance of assigned lab instruments, perform general lab duties, and contribute to training new team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present experimental results and progress updates at group meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to laboratory protocols, reports, and other documentation supporting process development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate effectively with team members and contribute to cross-functional activities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS degree in Chemistry, Biochemistry, or related field with minimum 2 years of industry experience, or MS degree with minimum 1 years of industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with laboratory-scale protein purification methods such as dialysis, diafiltration, and size-exclusion chromatography; experience with TFF is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of analytical methods including colorimetric assays, HPLC, SEC, and SDS-PAGE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with protein conjugation reactions or chemical modification of polysaccharides is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail, organizational skills, and record-keeping abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communication skills, both verbal and written.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work both independently and collaboratively in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enthusiasm for learning new skills and applying them to challenges outside of current expertise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to integrity, professionalism, and safety in all aspects of work.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Scientist, Conjugation Development\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12 Months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$51/hr. - $56/hr.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5210608008?gh_jid=5210608008","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":4469944008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5210608008,"updated_at":"2026-05-07T21:32:35-04:00","requisition_id":"T29-530-2026","title":"Associate Scientist II (Contract), Conjugation Development","company_name":"Vaxcyte","first_published":"2026-05-07T21:32:35-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking an Associate Scientist II (Contract), Conjugation Development, who will contribute to the development of a robust process for generating the company’s proprietary pneumococcal conjugate vaccine. This role will focus on the synthesis, purification, and analytical characterization of chemically modified polysaccharides and polysaccharide-protein conjugates. The successful candidate will apply a strong foundation in analytical chemistry and laboratory techniques to optimize and troubleshoot processes, while also supporting related areas such as analytical development and stability studies. This position requires strong organizational skills, clear communication, and the ability to work in a fast-paced, cross-functional environment.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform and optimize multi-step syntheses of protein-polysaccharide conjugates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Purify polysaccharides and conjugates using methods including dialysis, size-exclusion chromatography, and tangential flow filtration (TFF).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze polysaccharides and conjugates using methods such as colorimetric assays, HPLC assays, SEC-MALS, and SDS-PAGE, and contribute to method bridging studies and qualification to ensure robustness and consistency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate, well-organized experimental records and support data verification and analysis to enable process optimization and reproducibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with troubleshooting of synthesis, purification, and analytical procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track inventory of critical reagents and assist with ordering as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support maintenance of assigned lab instruments, perform general lab duties, and contribute to training new team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present experimental results and progress updates at group meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to laboratory protocols, reports, and other documentation supporting process development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate effectively with team members and contribute to cross-functional activities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS degree in Chemistry, Biochemistry, or related field with minimum 2 years of industry experience, or MS degree with minimum 1 years of industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with laboratory-scale protein purification methods such as dialysis, diafiltration, and size-exclusion chromatography; experience with TFF is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of analytical methods including colorimetric assays, HPLC, SEC, and SDS-PAGE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with protein conjugation reactions or chemical modification of polysaccharides is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail, organizational skills, and record-keeping abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communication skills, both verbal and written.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work both independently and collaboratively in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enthusiasm for learning new skills and applying them to challenges outside of current expertise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to integrity, professionalism, and safety in all aspects of work.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Scientist I, Conjugation Development\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12 Months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$51/hr. - $56/hr.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5224522008?gh_jid=5224522008","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":4476764008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5224522008,"updated_at":"2026-06-04T14:12:39-04:00","requisition_id":"T41-535-2026","title":"Associate Scientist II (Contract), Drug Product Analytics ","company_name":"Vaxcyte","first_published":"2026-05-20T21:57:04-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, including immunoassays, chromatography, spectrophotometric techniques, light scattering, and particle sizing. Experience in analyzing vaccine and adjuvant-containing formulations is a plus.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In addition, Vaxcyte is looking for an experienced and flexible individual who would be comfortable working on multiple projects at once, with fluid prioritization to enable aggressive timelines. This position is for a lab-based scientific role and requires excellent scientific judgement, independence, rigor, and thorough record-keeping.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Routine and non-routine analysis of internal release, development, and stability samples and reporting of data using multiple analytical techniques across the Drug Product working groups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Executing non-GxP stability study analysis for thermal, freeze/thaw, and agitation as well as container closure system evaluation for both Drug Substance and adjuvanted vaccine Drug Product materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Vaxcyte PCV products, external analytical, and manufacturing CMOs to enable tech transfer and implementation of processes and analytical methods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position is for a scientific role, which is predominantly lab-based, requiring excellent scientific judgement, independence, rigor, and thorough record-keeping.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS degree in Chemistry, Biochemistry, or related field with minimum 2 years of industry experience, or MS degree with minimum 1 years of industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The candidate will preferably have established practical experience in the analytical characterization of large biomolecular Drug Products in pre-filled syringes and vials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience executing bioanalytical components of stability studies and release tests.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in plate-based assays, immunoassay/ELISA, chromatography methods, spectrometric, and biophysical methodologies is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in authoring analytical technical documents, including method protocols, SOPs, and reports, as well as experience recording and templating electronic laboratory notebooks (eLN).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The candidate should have high degrees of both flexibility and organizational skills as well as an eagerness and ability to learn, to effectively navigate Vaxcyte’s multiple projects and timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills; ability to communicate effectively both verbally and in written formats are necessary to collaborate effectively with the rest of the Formulation and Drug Product Development team, as well as train other analysts and team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented, rigorous, and excellent skills in record keeping.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt; Senior Manager, Drug Product\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Onsite (minimum of 4 days per week).\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12months\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$51/hr. - $56/hr.\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5097117008?gh_jid=5097117008","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":4416593008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5097117008,"updated_at":"2026-04-09T20:06:47-04:00","requisition_id":"T20-610-2026","title":"Associate Scientist II (Contract), Research ","company_name":"Vaxcyte","first_published":"2026-01-26T21:05:45-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking an Associate Scientist II (contract), Research, to support the research and development of a novel bacterial polysaccharide conjugate vaccine. Specifically, this role will contribute to the setup, synthesis, purification, and analytical characterization of chemically modified polysaccharides and polysaccharide-protein conjugates.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will have an excellent understanding of conjugation process development, analytical chemistry principles, and substantial hands-on laboratory experience. The successful candidate will be expected to independently optimize and troubleshoot upstream and downstream conjugation processing procedures with minimal guidance. The candidate will also contribute across a range of related areas, including analytical development, stability studies, and process optimization initiatives. Responsibilities will also include record management, presenting data at group meetings, and contributing to the authorship of laboratory protocols and development reports.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Set up, optimize, and troubleshoot multi-step syntheses of protein-polysaccharide conjugates using click-chemistry and other related chemistries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Purify polysaccharides and conjugates using a variety of methods, including dialysis, FPLC chromatography, and tangential flow filtration (TFF).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Characterize protein/polysaccharide/conjugates using different analytical methods, including SDS-PAGE gel, Western blotting, ELISA, HPLC, SEC-MALS, colorimetric and dynamic binding assays, \u0026lt;em\u0026gt;et al\u0026lt;/em\u0026gt;.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply Design of Experiments (DoE) principles; design, execute, and interpret statistically modeled experiments using DoE software.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively contribute scientific ideas, experimental strategies, and process improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently review and summarize relevant scientific literature to inform experimental design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain highly organized records and Benchling entries to enable optimization and assessment of reproducibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze, interpret, and clearly communicate experimental data, including identifying trends, anomalies, and recommending next steps.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute established protocols with limited oversight, demonstrating strong technical proficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support team in routine laboratory activities and instrument maintenance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS. in Chemistry, Biochemistry, or related field or a related discipline, with minimum 2 years of relevant industry experience. MS without experience; or equivalent work experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of underlying scientific concepts, process development, and analytical assay principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive hands-on experience in purification methods such as diafiltration, depth filters, and TFF (required).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior hands-on experience in the conjugation process development is highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with common protein/polysaccharide/conjugates analytical techniques, including SDS-PAGE, Western blotting, ELISA, HPLC, and SEC-MALS, is required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of developing scalable processes suitable for the pharma/Biotech industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with vaccines, carbohydrates, or protein is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and excellent organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to contribute to the overall lab management, including organization of vendors, service contracts, and equipment maintenance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success working in a cross-functional team environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills, with excellent written and verbal communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Manager, Research\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12months\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;$51.00 - $56.00\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5250117008?gh_jid=5250117008","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":4487135008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5250117008,"updated_at":"2026-06-06T11:43:42-04:00","requisition_id":"T42-610-2026","title":"Associate Scientist II (Contract), Research ","company_name":"Vaxcyte","first_published":"2026-06-06T11:43:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte’s Research team uses a broad palette of chromatographic tools to purify diverse vaccine antigens. Applicants must have practical, hands-on experience with multiple chromatographic modalities (not limited to monoclonal antibody/Protein A workflows). Experience should include selection, screening, development, scale-up and characterization of various chromatography techniques.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute the following AKTA FPLC chromatography techniques:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Immobilized metal affinity chromatography (IMAC)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ion-exchange chromatography (IEX)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hydrophobic interaction chromatography (HIC)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Size-exclusion chromatography (SEC)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hydroxyapatite (CHT / HA)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Designing chromatography trains to reduce host cell protein, endotoxin and aggregates using complementary modalities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated DoE experience for multimodal optimization is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Membrane chromatography for high-throughput contaminant removal or virus/VLP processing and as a scale-friendly polishing/scavenging step.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Keep accurate and current records of development experiments and/or project related activities in an electronic laboratory notebook.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present data from experiments to the team and contribute to technical discussions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work within a team environment and provides support as necessary to further the team’s initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Biochemistry, Molecular Biology or a relevant science considered, with minimum of 2 years of relevant industry experience or MS with minimum of 1 year of relevant industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with diverse protein targets, bacterial and eukaryotic recombinant proteins, small/large subunit vaccine antigens, fusion proteins, multimeric complexes, glycoproteins, and VLPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The role requires demonstrated success with alternative capture/polishing methods and orthogonal cleaning strategies appropriate for potential vaccine antigens.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Preferred experience with Cell-free protein synthesis system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with automation or high throughput workflows such as (96-well plates) and UNICORN/AKTA software DoE integrations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in process development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills to collaborate well within the team and excellent written and verbal communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Scientist II, Research\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Onsite (minimum of 4 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026lt;/strong\u0026gt; 12months\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$51/hr. - $56/hr.\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5247253008?gh_jid=5247253008","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":4485779008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5247253008,"updated_at":"2026-06-05T12:50:35-04:00","requisition_id":"708-850-2026","title":"Corporate Affairs Associate","company_name":"Vaxcyte","first_published":"2026-06-05T12:50:35-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Corporate Affairs Associate is responsible for delivering clear, consistent, and engaging communications to internal and external stakeholders. This position provides hands-on experience across a range of communications activities, including content development, channel coordination, employee engagement initiatives, and external product communications support. The role is well suited for a highly organized, detail-oriented communicator eager to build foundational experience in corporate and product communications.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Internal Communications, Employee Engagement, Culture \u0026amp;amp; Community Support \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist in maintaining and updating the company intranet, including posting content, making minor updates, and supporting governance needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as main point of contact for incoming requests for internal communications support; draft and edit internal communications such as newsletters, announcements, recognition stories, and departmental messages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the internal communications content calendar by coordinating inputs, tracking deadlines, and assisting with reviews and quality checks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to All-Employee Meetings and leadership communications by helping prepare agendas, slides, speaker notes and supporting logistics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Update internal digital signage and assist with creating basic visual assets for internal campaigns, presentations, and meeting materials.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist with planning and communications for internal events, celebrations, and community engagement activities (e.g., Culture Club).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with external vendors to support internal programs and projects, including swag fulfillment, event logistics, employee photo shoots, and branded materials such as posters and environmental graphics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Gather participation data and feedback to support reporting and continuous improvement efforts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Corporate Affairs \u0026amp;amp; External Product Communications Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the development and execution of product communications plans leading up to and for Vaxcyte’s first potential product launch and additional key milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and contribute to the development of communications materials to support clinical and regulatory milestones, including press releases, Q\u0026amp;amp;As, presentations, and media briefing documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and draft content for owned digital channels such as LinkedIn and the corporate website.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help adapt internal stories and culture content for appropriate external audiences in alignment with corporate positioning and brand guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordination with media monitoring lead around key milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with the development and advancement of federal, state, and local policy strategies to support Vaxcyte’s pipeline, commercial strategy and long-term growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the development of briefing materials, policy positions and presentations tailored to federal and state stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide administrative and coordination support for broader Corporate Affairs initiatives as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Collaboration \u0026amp;amp; Professional Development\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work closely with cross-functional partners to support company-wide initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Learn and apply best practices in corporate communications, internal engagement, and external affairs through hands-on execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Take on project-based assignments that build foundational skills in writing, coordination, and stakeholder communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help ensure communications materials adhere to brand, tone, and visual identity guidelines across channels.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support content organization, asset management, and version control to ensure accuracy and consistency.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree with a minimum of 2-3 years of experience in a public relations or communications-related role; prior healthcare, biotech, pharma or PR agency experience desirable. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong writing and editing skills with the ability to simplify complex information.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with exceptional and meticulous attention to detail to manage and prioritize multiple competing projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Office (Word, PowerPoint, Excel) and basic design capability using Canva or Adobe Express.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills, diplomacy, and the ability to collaborate cross functionally with a solutions driven mindset.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Director, Product Communications\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy): \u0026lt;/strong\u0026gt;Hybrid (requires onsite presence at least three days per week).\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$93,000 - $109,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is not eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043040008,"name":"Corporate Affairs","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5173368008?gh_jid=5173368008","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":4453022008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5173368008,"updated_at":"2026-04-03T16:33:27-04:00","requisition_id":"741-820-B","title":"Director, Financial Planning \u0026 Analysis, R\u0026D","company_name":"Vaxcyte","first_published":"2026-04-03T16:33:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;This is an exciting opportunity to serve as a strategic finance business partner to Vaxcyte’s R\u0026amp;amp;D organization, with a focus on clinical studies. The role will support Clinical Operations and the Immunoassay and Non-Clinical teams, with responsibility for clinical trial and serology financial oversight, while flexing to support broader R\u0026amp;amp;D as business needs evolve. This individual will partner closely with Clinical Operations and Serology on planning, forecasting, accruals, financial reporting, and decision support across multiple development programs.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and provide strategic oversight for clinical outsourcing, partnering with Clinical Operations, Clinical Development, Finance, and Legal to assess the best fit for Vaxcyte’s pipeline and outsourced scope of work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the financial and commercial aspects of the RFP process, vendor selection, and budget management for the Clinical organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage clinical trials financial updates and support the annual planning process, including analysis of actuals versus forecast, risk and opportunity assessment, and clear reporting to Finance and business leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support contract and budget negotiations, bid evaluations, and vendor recommendations across a range of clinical service providers, including CROs, central laboratories, study supply vendors, oversight vendors, and patient recruitment partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist functional and department managers in the procurement process, including reviewing and validating invoices, supporting financial controls, and ensuring accurate visibility into vendor spend\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Operations, Clinical Development, Accounting, Procurement, Legal, and other stakeholders to align operational assumptions, vendor spend, timelines, and financial plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the clinical accrual process, including review of applicable CRO and other clinical ancillary vendor contracts. Collaborate with key stakeholders to gather and analyze relevant information to ensure all accruals are complete, accurately computed, documented, and recorded\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support program and project teams in identifying cost-saving opportunities, improving efficiencies, and optimizing the financial performance of clinical programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement new forecasting and analytics tools, enabling standardized metrics, scenario modeling, portfolio insights, greater transparency, and strategic decision support with an initial focus on clinical trials and serology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand and maintain Sarbanes-Oxley (“SOX”) documentation and requirements for assigned area\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead other ad hoc analysis to support business partnering as needs evolve\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Team Leadership\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is an individual contributor role that requires collaboration with Procurement, Clinical Operations, and R\u0026amp;amp;D leadership, as well as the ability to influence stakeholders without direct authority\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate leadership through proactive problem-solving, strong business partnership, and a continuous improvement mindset across financial planning, forecasting, and decision support activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;BA/BS in life sciences, technical, business, or a related field, advanced degree preferred with a minimum 12 years of progressive experience in biotech/pharma, including meaningful finance, FP\u0026amp;amp;A, clinical outsourcing, CRO, or related business-partnering experience. Other combinations of education and/or experience may be considered\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting Phase I-III clinical trials, including budgeting, forecasting, accruals, outsourcing, and vendor spend management, is required. Vaccines experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must possess strong analytical ability, a continuous learning mindset, and solid business acumen, including an understanding of business operations in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong negotiations, financial modeling, forecasting, and scenario-analysis skills, with the ability to translate complex operational inputs into clear financial insights and actionable recommendations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with ERP systems, financial planning tools, BI/analytics platforms, and AI-enabled productivity tools preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of US GAAP, financial reporting, accounting controls, and analytics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong relationship-building skills with internal and external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional project management skills, including the ability to prioritize, balance and manage multiple efforts with strong results/goal orientation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational, multi-tasking, listening, facilitation, and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work collaboratively across organizations and utilize resources effectively\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding written, verbal, and presentation skills, with the ability to convey strategies and results to a diverse audience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate effectively in a dynamic, fast-paced environment and flex across functions as business needs evolve\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Senior Director, FP\u0026amp;amp;A\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA; Onsite 3 days/week in San Carlos, with flexibility for remote work as needed.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$226,407 - $264,141 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043031008,"name":"Accounting \u0026 Finance","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5147570008?gh_jid=5147570008","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":4440460008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5147570008,"updated_at":"2026-05-01T19:55:44-04:00","requisition_id":"700-780-2026","title":"Director, Health Economics \u0026 Outcomes Research (HEOR)","company_name":"Vaxcyte","first_published":"2026-03-09T17:38:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking a Director, Health Economics \u0026amp;amp; Outcomes Research (HEOR) to establish and lead the company’s health economic strategy across the vaccine lifecycle, with initial focus on adult pneumococcal programs.\u0026amp;nbsp;This strategic leadership role will be responsible for developing and executing global health economic models to support payer value propositions, immunization policy engagement, reimbursement strategy, and external stakeholder communications.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role will focus specifically on health economic modeling and payer value strategy. Observational real-world evidence and epidemiology studies will be led by the Epidemiology \u0026amp;amp; Real-World Evidence function. The Director, HEOR will work in close collaboration with RWE and Epidemiology colleagues to ensure economic models are grounded in robust disease burden, vaccine effectiveness, and coverage assumptions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As Vaxcyte advances toward commercialization, this role will partner closely with Market Access colleagues, who will lead pricing and contracting strategy. The Director, HEOR will provide the analytic foundation and economic evidence required to inform pricing strategy, payer engagement, and health technology assessment discussions.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Health Economic Strategy \u0026amp;amp; Leadership\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and lead Vaxcyte’s HEOR strategy across early development, launch planning, and lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define the economic evidence generation plan required to support payer access and policy recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure health economic considerations are incorporated early into development planning.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Health Economic Modeling\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead development of cost-effectiveness, budget impact, and population health models for adult and pediatric vaccine programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and oversee decision-analytic models (e.g., Markov models, microsimulation models, dynamic transmission models as appropriate).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish modeling assumptions grounded in epidemiologic, clinical, and real-world data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all models are scientifically rigorous, transparent, and defensible in policy and payer environments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Value Communication \u0026amp;amp; Policy Support\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Translate health economic findings into clear, compelling value narratives for internal leadership and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development of global value dossiers, AMCP dossiers, and materials for payer engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to peer-reviewed publications and scientific congress presentations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Cross-Functional Partnership\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Epidemiology \u0026amp;amp; RWE to integrate disease burden and vaccine effectiveness assumptions into economic models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Clinical Development, Regulatory, Medical Affairs, and Market Access teams to align value strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support consistent, aligned value messaging across stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Capability Building\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish best practices and governance processes for health economic modeling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and manage external modeling partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mentor future HEOR team members as the function expands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;PhD in Health Economics, Health Services Research, Public Health, Epidemiology, or related quantitative field with 8+ years of relevant industry experience required OR Master’s degree (e.g., MPH, MSc, MBA) with 12+ years of relevant industry experience in health economic modeling.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading cost-effectiveness and budget impact models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in decision-analytic modeling methodologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting payer submissions or health technology assessments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional leadership and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Vice President, Scientific Affairs \u0026amp;amp; Epidemiology\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA/Remote (US)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$242,000 – $282,000 *(SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4074311008,"name":"Scientific Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5131868008?gh_jid=5131868008","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":4433522008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5131868008,"updated_at":"2026-06-03T16:09:40-04:00","requisition_id":"688-515-2026","title":"Director, Immunoassay Development","company_name":"Vaxcyte","first_published":"2026-02-25T20:47:31-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking an accomplished Director, Immunoassay Development to establish and lead a dedicated analytical function focused on immunoassay development for complex conjugated vaccines. This role will build and manage a laboratory-based team responsible for developing, sustaining, and continuously improving potency- and antigenicity-based immunoassays to support CMC development from preclinical through BLA-stage programs and commercialization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A key initial focus of this role will be stewardship of the VAX-31 MSD immunoassay platform, which has been developed and advanced to Phase 3 through extensive internal leadership spanning clinical serology, GLP studies, and immunoassay development. The successful candidate will work in close partnership with current immunoassay leadership to ensure comprehensive knowledge transfer, continuity of scientific and execution excellence, and the long-term robustness of the immunoassay strategy as accountability and responsibility intentionally transition into Analytical Development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a hands-on scientific leadership role anchored in CMC execution, GMP readiness, and lifecycle management of immunoassays supporting vaccine development, lot release and stability testing and commercialization.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Help establish, lead, and scale the Immunoassay capability within Global Analytical Development, including defining scope, operating model, technical standards, platform strategy, outsourcing approach, validation support model, routine testing model, and control strategy priorities aligned with CMC and program needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide daily laboratory leadership, including experimental planning, laboratory schedule coordination, study prioritization, reagent and sample readiness, data review, documentation expectations, instrument and workflow oversight, and hands-on technical support to ensure high-quality execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, mentor, and manage a laboratory-based team of scientists responsible for immunoassay development, optimization, troubleshooting, qualification support, method transfer, validation support, routine analytical testing, lifecycle management, and continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strengthen Vaxcyte\u0026#39;s immunoassay portfolio by developing fit-for-purpose immunoassays that support potency, antigenicity, identity, impurity, characterization, comparability, release, stability, and lifecycle needs across the vaccine pipeline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide hands-on scientific leadership for assay design, sample preparation strategy, reagent strategy, plate or bead format selection, signal detection approach, data analysis model, system suitability expectations, and robustness assessment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead structured immunoassay troubleshooting and root-cause analysis for assay variability, reagent performance, sample preparation, matrix effects, antigen accessibility, signal response, curve behavior, recovery, precision, specificity, robustness, and long-term method trending.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and implement innovative or alternative immunoassay technologies, including ELISA, MSD, Luminex, automation-enabled workflows, and other relevant ligand-binding assay formats.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop new immunoassay methods from concept through optimization, qualification readiness, transfer readiness, validation readiness, and lifecycle strategy, including control strategy considerations and documentation suitable for CMC decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strengthen immunoassay analytical control strategies, including critical reagent strategy, reference material strategy, assay controls, system suitability, sample preparation, acceptance criteria, bridging approaches, trending, stability planning, and lifecycle monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee outsourced immunoassay activities with CROs, CDMOs, contract testing laboratories, reagent vendors, and external technology partners, including technical scope definition, study design review, data review, vendor performance oversight, and deliverable acceptance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support immunoassay method validation activities in partnership with ASAT, QC, Quality, Regulatory, and external testing partners, including validation strategy, protocol input, acceptance criteria, data interpretation, deviation support, and final report review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support routine immunoassay testing needs within the CoE, including development-stage testing, characterization testing, platform evaluation studies, method bridging, comparability support, reagent qualification, and other non-GMP or GMP-supporting analytical activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support QC and ASAT teams in technical questions related to release, stability, comparability, PPQ, method transfer, validation readiness, and commercial readiness activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop phase-appropriate immunoassay strategies across the vaccine pipeline, ensuring methods and control strategies are aligned with preclinical, clinical, late-stage, BLA, commercial, and lifecycle needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage immunoassay development, outsourcing, validation-support, routine testing, and platform innovation activities across multiple projects, including resource planning, timeline management, deliverable tracking, and risk escalation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish a high-performing laboratory culture grounded in scientific rigor, accountability, collaboration, transparency, data integrity, hands-on problem solving, operational discipline, and continuous learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to regulatory submissions, health authority responses, technical reports, method development reports, validation strategies, comparability packages, platform evaluation summaries, and BLA-supporting documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Immunoassay Development in technical governance forums, program teams, cross-functional reviews, vendor discussions, and external collaborations as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD. in Biochemistry, Immunology, Analytical Chemistry, Biological Sciences, or a related field (or equivalent experience) with a minimum of 10 years of experience. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated scientific depth, independent immunoassay development leadership, complex troubleshooting experience, and ability to lead cross-functional technical workstreams are required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant hands-on, lab-based experience developing, optimizing, troubleshooting, transferring, validating, lifecycle-managing, and executing immunoassays in vaccine CMC, biologics analytical development, QC, ASAT, or other regulated analytical environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise in immunoassay method development, including assay format selection, reagent strategy, sample preparation, assay optimization, robustness assessment, qualification, validation readiness, method transfer, and lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong technical experience with ligand-binding immunoassay platforms such as ELISA, MSD, ELISA, Luminex, or other relevant immunoassay technologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to troubleshoot complex immunoassay performance trends using structured, data-driven root-cause analysis approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience evaluating alternative or innovative immunoassay platforms and translating platform learnings into fit-for-purpose analytical strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing or improving potency, antigenicity, identity, or impurity assays supporting vaccine or biologics release, stability, comparability, process development, method transfer, validation, routine testing, or regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience overseeing outsourced immunoassay activities, including CRO, CDMO, contract testing laboratory, reagent vendor, or external technology partner interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage daily laboratory operations, including study planning, staff planning, sample and reagent readiness, testing prioritization, data review, documentation, and technical support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience with conjugated vaccines, polysaccharide-protein conjugates, multivalent vaccines, or other complex biologics is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of protein chemistry, polysaccharide chemistry, conjugation chemistry, antigen structure, antibody-antigen interactions, and biological sample matrix effects as applied to vaccine analytical development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with MSD platforms is highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with Luminex or other multiplex immunoassay platforms is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in or supporting GMP-regulated analytical environments is desired, including familiarity with method qualification, validation, transfer, change control, deviations, investigations, CAPA, data integrity, and lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of global regulatory expectations for analytical methods supporting vaccines and biologics, including FDA, EMA, ICH, and GMP expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading, mentoring, and developing laboratory scientists, including building team capability, setting priorities, managing performance, providing technical coaching, and fostering a collaborative culture.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to manage multiple technical workstreams, outsourced activities, validation-support activities, routine testing needs, resources, timelines, and deliverables in a fast-paced, matrixed environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific judgment and the ability to make sound technical recommendations when working with incomplete, complex, or conflicting data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, with the ability to clearly communicate complex technical concepts to cross-functional stakeholders, senior leaders, external partners, and regulatory audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong commitment to data integrity, documentation quality, scientific excellence, accountability, and continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Preferred Qualifications:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting late-stage development, PPQ readiness, BLA preparation, commercial launch, or lifecycle management of vaccine or biologics programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience supporting analytical methods used for GMP release and stability testing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with immunoassay transfer, validation, bridging, comparability, critical reagent qualification, reference material qualification, and long-term method performance monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing outsourced immunoassay development, validation, platform evaluation, or routine testing activities with external laboratories or technology partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing alternative or next-generation immunoassay methods to strengthen analytical capability and support long-term control strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience interacting with global health authorities on analytical, potency, antigenicity, or immunoassay-related topics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building or scaling analytical capabilities, Centers of Excellence, or laboratory teams within a growing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with multivalent or highly complex vaccine programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automation, high-throughput immunoassay workflows, multiplex assay design, LIMS, ELN, and digital data analysis tools.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Director, Commercial Readiness and Analytical Strategy\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy): \u0026lt;/strong\u0026gt;Onsite (minimum of 4 days per week)\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA (Onsite, laboratory-based leadership role)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$213,000 – $250,000\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043044008,"name":"Analytical","child_ids":[],"parent_id":4043043008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/4612434008?gh_jid=4612434008","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":4210257008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Full-time","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":4612434008,"updated_at":"2026-03-09T18:31:21-04:00","requisition_id":"3","title":"Don't see a role you're looking for? Please submit your resume for future consideration","company_name":"Vaxcyte","first_published":"2025-03-31T21:12:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div\u0026gt;At Vaxcyte, we are always looking for bright, committed, and innovative people who are passionate about making a difference.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;If you do not see an opportunity on our Careers Page that is a good match with your background, please submit your resume to be part of our Talent Community to be considered for future opportunities.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;We also encourage you to regularly visit our \u0026lt;a class=\u0026quot;postings-link\u0026quot; href=\u0026quot;https://jobs.lever.co/vaxcyte\u0026quot;\u0026gt;Careers Page\u0026lt;/a\u0026gt; as we continue to grow and add more opportunities.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052735008,"name":"Talent Community","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5176025008?gh_jid=5176025008","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":4454195008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5176025008,"updated_at":"2026-05-27T12:41:33-04:00","requisition_id":"T33-520-2026","title":"Engineer II, Upstream Development for Protein Development and Manufacturing (Contract)","company_name":"Vaxcyte","first_published":"2026-04-03T22:59:34-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking a talented and experienced Engineer II, to join the Upstream Process Development group within the Protein Development and CMC team. This is an exciting opportunity to join an outstanding team pursuing bacterial fermentation development at Vaxcyte.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful candidate will have the following skills and qualities:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience operating and maintaining bioreactors, including Ambr® 250, at laboratory scale.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with pilot scale fermentation and recovery equipment is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skillful in analyzing and presenting data for process improvements, troubleshooting, and optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An exceptional team player who works seamlessly with others, speaks up, and remains focused on achieving the best results to achieve company goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and planning skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead operational activities related to bioreactor set-up, monitoring, harvest, and maintenance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, test, and implement recipe scripting for fed-batch fermentation feeding controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide engineering support for design, implementation, and qualification of scale-down models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author SOPs (standard operating procedure), process flow diagrams and batch records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze and present fermentation data at internal project meetings. Participate in upstream database management and documentation in electronic notebooks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Chemical Engineering or a related discipline with 10+ years, MS with 7+ years, or PhD with 2-5 years of relevant Pharma/Biotech industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with fermentation and/or primary recovery unit operations.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Good understanding in fundamentals of bioreactor design, operation and controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of aseptic techniques\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mechanical and technical knowledge of primary recovery unit operations such as homogenization, centrifugation, and depth filtration, is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of fermentation scale up and development of scale down models\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with DoE (Design of Experiments) principles and software.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements of biotherapeutics. Late-stage process characterization experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Senior Scientist, Upstream Development for Protein Development \u0026amp;amp; Manufacturing\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;12 months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$70.00 - $78.00\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5231879008?gh_jid=5231879008","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":4480386008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5231879008,"updated_at":"2026-05-29T12:44:30-04:00","requisition_id":"747-720-B","title":"Executive Director Quality Assurance, External Manufacturing ","company_name":"Vaxcyte","first_published":"2026-05-29T12:44:30-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Executive Director, Quality Assurance, External Manufacturing is responsible for leading the External Manufacturing Quality function and executing the quality strategy across Vaxcyte’s global network of Contract Development and Manufacturing Organizations (CDMOs) and external partners. In a highly outsourced operating model, this role ensures that externally executed GMP activities are compliant with global regulatory requirements and Vaxcyte quality standards, supporting product quality, supply continuity, and regulatory readiness.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This leader drives a proactive, risk-based quality approach and implements scalable systems, governance, and partnerships to enable operational excellence across the external network, supporting clinical development, BLA readiness, and commercial supply. The Executive Director owns external quality performance and operational decision-making within the function, while escalating critical risks and aligning with VP-level strategy. This role requires strong cross-functional leadership and the ability to influence internal and external stakeholders in a highly matrixed environment.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own quality performance across the external network, ensuring compliance, supply continuity, and effective management of quality risk, with escalation of critical risks to VP-level as appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide end-to-end QA leadership for externally executed GxP activities, including manufacturing and release of drug substance, drug product, components, and critical raw materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the senior QA leader for external operations, representing Quality in cross-functional and executive forums, and influencing decisions across Technical Operations, CMC, Regulatory, and Supply Chain.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain strategic partnerships with external partners, driving accountability, performance management, and continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead quality governance across the external network, including KPIs, escalation pathways, and risk-based oversight models focused on critical processes and high-risk partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and drive resolution of complex, cross-organizational quality issues, ensuring robust investigations, root cause analysis, and sustainable CAPAs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight and decision authority for batch disposition and product release, ensuring timely, compliant supply of clinical and commercial materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive inspection readiness across the external network, including PAI and global health authority inspections, and serve as a key QA representative during inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic QA leadership for technology transfer, process validation, and lifecycle management across external sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, lead, and develop a high-performing External Quality organization, including talent development, succession planning, and organizational scalability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion a strong quality culture across internal teams and external partners, reinforcing accountability, transparency, and continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;BS/BA required, with a minimum of 16 years of progressive experience in Quality Assurance within biopharmaceuticals, including significant leadership in external manufacturing and CDMO oversight, vaccines experience desirable. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in GMP regulations, FDA and global regulatory expectations, and ICH guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience operating within a highly outsourced/CDMO-based manufacturing model\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of leading complex external quality networks, driving performance and outcomes without direct authority\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience supporting technology transfer, process validation, and lifecycle management across multiple external sites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success in inspection readiness and regulatory inspections, including pre-approval inspections (PAIs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience establishing governance frameworks, and performance metrics for external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong background in risk management and quality systems, with the ability to apply risk-based decision-making in a GxP environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to influence at the executive level, driving alignment across cross-functional teams and external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience building, leading, and scaling high-performing teams in a complex, fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong business acumen, with the ability to balance quality, compliance, and supply continuity to support\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;clinical and commercial objectives\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Competencies \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic Leadership in Outsourced Models\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;External Partner Governance \u0026amp;amp; Influence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Risk-Based Quality Oversight\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Regulatory Inspection Readiness (PAI Focus)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Executive Communication \u0026amp;amp; Cross-Functional Leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complex Problem Solving \u0026amp;amp; Decision-Making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organizational Development \u0026amp;amp; Talent Leadership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Vice President, Quality Assurance\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Hybrid (minimum of 2-3 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$300,000 - $350,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is not eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043053008,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5197498008?gh_jid=5197498008","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":4463839008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5197498008,"updated_at":"2026-05-01T16:12:58-04:00","requisition_id":"719-920-2026","title":"Manager, IT Quality \u0026 Compliance","company_name":"Vaxcyte","first_published":"2026-04-23T18:00:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte’s IT team is seeking a motivated, forward-thinking Manager, IT Quality \u0026amp;amp; Compliance to support executing and supporting IT Quality, Compliance, and Validation (CSV/CSA) activities across GxP systems. This role partners closely with the Director of IT Quality \u0026amp;amp; Compliance to operationalize the IT QSC (Quality, Security, Compliance) strategy and ensure systems remain compliant, secure, and audit-ready.\u0026amp;nbsp;This is a hands-on role requiring expertise in IT system validation, auditing, vendor management, and compliance operations within a regulated GxP environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Functions:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;IT Validation \u0026amp;amp; CSV/CSA Execution\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute Computer Software Assurance (CSA) and Computer System Validation (CSV) activities for GxP systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support validation lifecycle activities (planning, testing, documentation, release, and change management).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ITQA oversight for implementation of GxP systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support data migration validation (reconciliation, traceability, and verification).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Audit \u0026amp;amp; Inspection Readiness\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform internal IT CSV audits to ensure regulatory and procedural compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and execute GxP vendor audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare audit documentation, evidence packages, and formal audit reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support regulatory inspections and inspection readiness activities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Vendor Management \u0026amp;amp; Oversight\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Conduct vendor qualification and periodic vendor audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support vendor risk assessments and compliance monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure vendors meet GxP, data integrity, and security requirements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Periodic Reviews \u0026amp;amp; Compliance Monitoring\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform periodic reviews of GxP systems to maintain validated state.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify compliance gaps and drive remediation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support continuous audit and compliance monitoring programs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Investigations \u0026amp;amp; CAPA Management\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support IT investigations (deviations, incidents, compliance gaps).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and manage CAPAs, ensuring timely closure and effectiveness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally to implement corrective and preventive actions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Documentation \u0026amp;amp; SOP Development\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Author and maintain IT and QA SOPs, policies, and work instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment with GxP and 21 CFR Part 11 requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support continuous improvement of documentation and processes.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Data Integrity, Cybersecurity \u0026amp;amp; Infrastructure Alignment\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support implementation of data integrity controls (ALCOA+).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with IT Security to align compliance with cybersecurity controls (access, logging, monitoring).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure infrastructure supporting GxP systems is maintained in a secure and compliant state (patching, backup, recovery).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and escalate risks related to data integrity, cybersecurity, and infrastructure.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Training \u0026amp;amp; Cross-Functional Collaboration\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support IT Quality \u0026amp;amp; Compliance training initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate across IT, Security, Quality, and business teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Promote a culture of compliance, quality, and audit readiness.\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 IT, Quality, Life Sciences, or related field and minimum 5 years of experience in IT Quality, CSV/CSA, or compliance in a GxP environment. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;IT system validation (CSV/CSA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Internal and vendor audits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Periodic reviews of GxP systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Vendor management and oversight\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data migration validation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting or working with laboratory (GxP lab) and manufacturing systems (e.g., MES, LIMS, lab instruments)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Veeva, ERP systems, or regulated SaaS platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting or implementing GxP systems from a QA perspective\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of GxP, 21 CFR Part 11, and data integrity principles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience authoring SOPs, validation documentation, CAPAs, and investigations\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 life sciences or biotech environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience writing and presenting audit reports and familiarity with risk management frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to QSC (Quality, Security, Compliance) integration and knowledge of data governance and data integrity practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of cybersecurity (access control, data protection, incident response).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to IT security and infrastructure controls (patching, system hardening).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using AI tools for research, analysis, and process optimization.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Director, IT Quality \u0026amp;amp; Compliance\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Open to Remote; San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$169,000 - $198,00 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043035008,"name":"IT","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5155640008?gh_jid=5155640008","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":4444495008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5155640008,"updated_at":"2026-03-25T12:12:40-04:00","requisition_id":"682-720-2026","title":"Manager, Quality Assurance, Compliance","company_name":"Vaxcyte","first_published":"2026-03-25T12:12:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking a Manager, Quality Assurance, Compliance who is responsible for providing day-to-day operational oversight\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;governance and strategic oversight of key Quality System processes, with a primary focus on leading Change Control governance and deviation/investigation oversight\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;review board leadership.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;This role insures consistent, risk-based decision making, inspection readiness, and cross-functional accountability across quality systems. The Manager acts as an operational backbone\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;a governance leader for cross-functional quality processes, proactively identifying systemic risks, ensuring procedural compliance, driving performance through KPIs, and presenting quality system health and trends through Management Review.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Change Control Governance \u0026amp;amp; Board Leadership\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and coordinate the Change Control Review Board (CCRB), including agenda development, facilitation, quorum confirmation, and documentation of decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform pre-CCRB QA review of Change Requests to ensure completeness, clarity, and appropriate risk classification prior to board review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verify alignment of Change Requests with applicable SOPs, including confirmation of CCRB-required versus discretionary changes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide QA authority on change classification, risk assessment, impact evaluation, and implementation strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own CCRB performance metrics, including cycle time, risk categorization trends, backlog, and recurring impact areas. Present trends and risk signals to senior leadership and during Management Review.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Deviation and Investigation Governance\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead or co-lead Deviation Review Boards to ensure consistent, risk-based decision making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure appropriate classification (minor, major, critical) and scientifically sound investigations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate adequacy of root cause analyses (e.g., 5-Why, Fishbone).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure linkage between deviations, CAPA, and change controls to prevent recurrence and address systemic risk.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Quality Metrics and Management Review\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own development, maintenance, and reporting of Quality System KPIs related to Change Control, Deviations, Investigations, and CAPA.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform routine trend analysis and signal detection to identify emerging compliance risks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present Quality System performance data during Management Review.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Inspection Readiness and Regulatory Support\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as Subject Matter Expert (SME) for Change Control and Deviation processes during regulatory inspections and audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation of audit responses and ensure timely and compliant closure of observations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain processes in a continuous state of inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of experience in Quality Assurance within the pharmaceutical, biotechnology, or medical device industry. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading cross-functional governance boards strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of ICH Q10, risk management principles, and inspection expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with electronic Quality Management Systems (eQMS) strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth knowledge of cGMP regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills, attention to detail, and ability to manage multiple priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal and communication skills to work effectively across functions and with external partners.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Associate Director, QA, Compliance\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA; Hybrid\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$151,000 – $176,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043053008,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5202025008?gh_jid=5202025008","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":4465859008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5202025008,"updated_at":"2026-05-05T11:44:19-04:00","requisition_id":"683-720-2026","title":"Manager, Quality Assurance, External Manufacturing","company_name":"Vaxcyte","first_published":"2026-04-29T17:58:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Manager, Quality Assurance, External Manufacturing is responsible for overseeing quality activities at contract manufacturing organizations (CMOs), ensuring compliance with cGMP standards, and driving performance through KPIs and continuous improvement initiatives. This role leads batch disposition, reviews critical GMP documentation, supports PPQ activities, and collaborates cross-functionally to resolve complex manufacturing and quality issues. The position requires strong expertise in pharmaceutical quality systems, regulatory requirements, and risk management, along with leadership, problem-solving, and communication skills to support both clinical and commercial operations.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide Quality Assurance oversight of Contract Manufacturing Organizations (CMOs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and report metrics and key performance indicators (KPIs) to evaluate CMO performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Quality Assurance at internal cross-functional meetings and Joint Project Team meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead polysaccharide batch disposition activities, including review of executed batch records, environmental monitoring data, and quality control results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve GMP documentation, including master batch records, deviations, risk assessments, change controls, and CAPAs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive resolution of quality performance issues in collaboration with contract manufacturers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Process Performance Qualification (PPQ) activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, implement, and maintain quality procedures, policies, and standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with key stakeholders to develop solutions to complex manufacturing and quality issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in compliance audits and regulatory inspections, as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Promote a strong quality mindset and a culture of quality excellence across all activities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in chemistry, Biology, Pharmacy, Engineering, or a related scientific discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5 years of experience in managing CMO quality, and quality systems management within the pharmaceutical, biotechnology, or life sciences industry. Other combinations of education and experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in batch record review, deviations and Out of Specification (OOS) investigations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough knowledge of cGMP, ICH guidelines, FDA/EMA, Swiss medic regulations, and international pharmaceutical quality standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience applying Quality Risk Management principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting both clinical and commercial products preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership, management, and process improvement skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills with strong attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of biologics manufacturing operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to prioritize multiple assignments in a fast-paced, changing environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving abilities, including managing complex investigations and root cause analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, with the ability to clearly present quality topics and risk-based decisions to cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Director, Quality Assurance\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Open to Remote;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$151,000 – $176,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043053008,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5195807008?gh_jid=5195807008","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":4463053008,"location":{"name":"US - Remote"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Remote","value_type":"single_select"}],"id":5195807008,"updated_at":"2026-05-04T15:06:35-04:00","requisition_id":"693-770-2026","title":"Medical Science Liaison","company_name":"Vaxcyte","first_published":"2026-04-27T19:56:30-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;We are\u0026amp;nbsp;seeking\u0026amp;nbsp;a scientifically driven and communicative Medical Science Liaison (MSL) to join our Medical Affairs team.\u0026amp;nbsp;The Medical Science Liaison (MSL) serves as a scientific expert in immunization and\u0026amp;nbsp;pneumococcal\u0026amp;nbsp;disease prevention. This field-based role\u0026amp;nbsp;will serve as a trusted scientific partner to\u0026amp;nbsp;healthcare providers, public health officials, and\u0026amp;nbsp;key opinion leaders (KOLs)\u0026amp;nbsp;to support vaccine education, clinical development, and real-world evidence generation.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134245417\u0026amp;quot;:false,\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Depending on experience, the role may be leveled at Senior MSL, offering expanded responsibilities in strategic leadership and mentorship.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134245417\u0026amp;quot;:false,\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Stakeholder Management: Build and maintain scientific relationships with key opinion leaders, clinicians, researchers, and public health stakeholders.\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Scientific Engagement: Communicate epidemiological, clinical and real-world data regarding pneumococcal disease and Vaxcyte’s candidate vaccine.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Evidence Generation Support: Where relevant, support investigator-initiated studies and clinical trial recruitment in vaccine research.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Insight Collection and cross-functional collaboration: Gather and share field insights on pneumococcal disease landscape, vaccine data needs, and recommendation scenarios.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Education and Engagement: Represent the company at scientific meetings, conferences, and stakeholder events.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Compliance: Uphold ethical standards and regulatory guidelines in all field activities.\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;134245417\u0026amp;quot;:false,\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:0,\u0026amp;quot;335559740\u0026amp;quot;:288}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Advanced degree (PhD, PharmD, MD, MPH) in life sciences, immunology, or public health\u0026amp;nbsp;preferred.\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;A minimum of 5 years of experience in medical affairs, clinical research, or infectious disease.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Strong knowledge of immunology and vaccine development.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Excellent communication skills with ability to address scientific and public health audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Travel: MSL positions are field-based and require significant travel, which can vary depending on the assigned territory. \u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Ability to travel up to 70% of the time.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Other combinations of education and/or experience may be considered.\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Senior Director, Medical Affairs\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Remote - United States\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$184,000 - $215,000\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4074310008,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4060325008,"name":"US - Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5190224008?gh_jid=5190224008","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":4460353008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5190224008,"updated_at":"2026-05-01T16:32:18-04:00","requisition_id":"686-750-2026","title":"Project Manager","company_name":"Vaxcyte","first_published":"2026-04-21T11:39:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte has an opportunity for a Project Manager to manage complex, cross‑functional initiatives focused on IT and Finance Systems implementations, ensuring smooth delivery across planning, requirements, system design, testing, deployment, training, and change management. This leader partners closely with finance teams, operations, IT, and vendors to deliver technology solutions that improve data integrity, operational efficiency, and strategic decision‑making.\u0026amp;nbsp;Reporting into the Associate Director of Project Management, the ideal candidate will bring experience managing cross-functional teams, a deep understanding of financial and system implementation workflows, and the ability to drive clarity, alignment, and execution across diverse stakeholder groups.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support day-to-day project management activities for ERP implementation, with a focus on Finance, Supply Chain, and Data/Analytics workstreams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and manage recurring meetings, including scheduling, agenda preparation, and documentation of meeting minutes and action items\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and update key project management artifacts, including the project plan, RAIDD log (Risks, Assumptions, Issues, Dependencies, Decisions), and status tracking tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and update weekly and monthly project status reports and presentation materials for leadership and stakeholder updates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor progress across assigned workstreams, proactively identifying risks, issues, and dependencies, and escalating as appropriate\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a communication liaison between workstream leads and program leadership to ensure alignment and timely information flow\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in core team and cross-functional meetings, ensuring accurate roll-up of status, risks, and key decisions to program leadership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in project management, information technology, or a related field. Master’s degree preferred. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5 years of project management experience in IT system implementations, including work with finance applications. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in biotechnology, pharmaceuticals, medical devices, or other regulated scientific environments preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with change management frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with GxP validation practices and documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success leading multiple projects in complex, multi‑stakeholder organizations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with supply chain, finance, and IT teams simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of financial processes (budgeting, GL, AP/AR, procurement, reporting) and laboratory workflows (sample lifecycle, instrument data, QA/QC, data integrity).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced proficiency in Smartsheet, including; Complex project plan development, Automation workflows, portfolio and executive‑level dashboards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to build dashboards and reporting\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;tools that summarize health, risks, KPIs, and resource status for leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level of organization, analytical thinking, resourcefulness, and problem‑solving.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to thrive in dynamic, high‑growth environments with evolving priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills, with the ability to engage and influence stakeholders at all levels.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Associate Director, Project Management\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$148,000 - $173,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043042008,"name":"Project Management","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5168618008?gh_jid=5168618008","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":4450720008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5168618008,"updated_at":"2026-05-12T18:00:27-04:00","requisition_id":"T31-515-2026","title":"Scientist I (Contract), Analytical Development","company_name":"Vaxcyte","first_published":"2026-04-01T20:04:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte has an exciting opportunity for an energetic and talented individual to join our Analytical Development team. The Scientist I, Analytical Development, is responsible for executing analytical testing and contributing to analytical method development activities for biologics/vaccine development programs.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;This role performs routine and non-routine analytical assays using modern analytical techniques, supports method optimization and troubleshooting efforts, and contributes to continuous improvement initiatives with moderate supervision while partnering effectively with cross-functional teams. The position requires demonstrated hands-on laboratory experience, strong technical execution, and problem-solving skills, with the ability to independently plan and execute assigned work, analyze and interpret data, and escalate and/or drive investigations as needed. This role authors and maintains clear technical documentation, including method protocols, method development summaries, and SOPs, and communicates experimental results and conclusions to internal stakeholders.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Method Development \u0026amp;amp; Troubleshooting\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to method development, optimization, and qualification/validation readiness activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and execute experiments to evaluate critical method parameters and define appropriate system suitability and control strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot assay and instrument performance issues using a structured approach; interpret data to identify likely root causes, implement corrective actions, and document outcomes and recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and/or execute method transfer activities, including protocol preparation, training support, execution at receiving labs, and resolution of transfer issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and revise analytical methods, SOPs, protocols, and technical reports; ensure clear documentation of experimental rationale, results, and conclusions for internal review and stakeholder communication.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Team Collaboration\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner effectively with cross-functional teams to define analytical plans, meet project timelines, and deliver high-quality outputs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate experimental progress, data interpretation, and emerging risks clearly; propose mitigation plans and align next steps with stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to a compliant, safety-focused, and scientifically rigorous lab culture, model good documentation practices and data integrity expectations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Analytical Testing \u0026amp;amp; Data Generation\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine and non-routine analytical testing using modern analytical methods (e.g., HPLC/UPLC, SEC, CE, UV-Vis, ELISA, electrophoresis, plate-based assays, and other biochemical/biophysical techniques).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute assays in accordance with approved methods, SOPs, and applicable quality standards (GLP/GMP as applicable); identify and troubleshoot common issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform data processing and interpretation; summarize results, trends, and potential risks, and escalate complex findings for review and decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate, timely documentation in laboratory notebooks or electronic systems; contribute to clear technical communications to project and cross-functional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Laboratory Operations \u0026amp;amp; Instrumentation\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Coordinate routine instrument maintenance and service activities; interface with vendors as needed and support timely issue resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure laboratory organization, cleanliness, and compliant material labeling/storage practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage inventory of reagents, standards, and consumables; initiate procurement, track critical supplies, and support forecasting to avoid stockouts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Safety \u0026amp;amp; Compliance\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Follow all Environmental Health \u0026amp;amp; Safety (EHS) policies and laboratory safety practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Handle chemicals and biological materials safely and in compliance with regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure proper waste disposal and adherence to hazardous material handling procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support audit and inspection readiness activities where applicable.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;PhD, MS or Bachelor’s degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline. PhD with 1-2 years; MS with 5+ years; BS with 8+ years of relevant industry experience in analytical development, QC, or related field. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong hands-on experience with multiple analytical techniques, such as UV-Vis, HPLC, CE, SDS-PAGE, icIEF, Liquid chromatography, Mass Spectrometry, enzyme kinetics, colorimetric and fluorescent plate-based assays, ELISA, Western Blot, and PCR.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience independently driving method development or optimization activities preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of analytical chemistry/biochemistry principles with demonstrated application to assay development and control strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to independently troubleshoot non-routine assay and instrument issues using structured root-cause analysis and data-driven decision making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in analytical software, data processing workflows, and statistical tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific judgment and attention to detail consistently produces high-quality, inspection-ready documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to independently plan and prioritize work, manage multiple projects, and meet timelines with minimal supervision.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear and effective written and verbal communication; able to summarize complex data, present recommendations, and collaborate across functions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Senior Manager, Analytical Development\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;6months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$62.00/hr. - $68.00/hr. (SF Bay Area).\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5224535008?gh_jid=5224535008","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":4476769008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5224535008,"updated_at":"2026-06-05T19:36:00-04:00","requisition_id":"T42-535-2026","title":"Scientist I (Contract), Drug Product Analytics","company_name":"Vaxcyte","first_published":"2026-05-20T21:57:35-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, especially immunoassays and multiplexed immunoassay formats. Experience in analyzing vaccine and adjuvant-containing formulations is a plus.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In addition, Vaxcyte is looking for an experienced and flexible individual who would be comfortable working on multiple projects at once, with fluid prioritization to enable aggressive timelines. This position is for a lab-based scientific role and requires excellent scientific judgement, independence, rigor, and thorough record-keeping.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute routine and non-routine analysis of internal release, development, and stability samples using a variety of analytical techniques across Drug Product working groups, ensuring high-quality data generation and reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the execution, optimization, and continuous improvement of Vaxcyte’s internal multiplex immunoassay (MSD) assay suite, including troubleshooting assay performance, improving robustness, and supporting assay lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design, execute, and interpret experiments to support non-GxP stability studies including thermal, freeze/thaw, agitation, and container closure system evaluations for both Drug Substance and adjuvanted vaccine Drug Product materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze and interpret complex assay data, identify trends or deviations, and communicate findings to project teams to support development decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to method development, qualification, and technology transfer activities, including collaboration with external analytical laboratories and manufacturing CMOs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review technical documentation including assay protocols, SOPs, reports, study plans, and technical summaries in support of development and analytical activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Vaxcyte PCV and VAXA1 programs through cross-functional collaboration with Drug Product Development, Formulation, Analytical Development, Quality, and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Vaxcyte is seeking a flexible and collaborative scientist comfortable managing multiple priorities in a fast-paced development environment. This role is predominantly lab-based and requires strong scientific judgment, independence in experimental execution, rigor in data analysis, and meticulous record keeping.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD, MS or Bachelor’s degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline. PhD with 1-2 years relevant industry experience; MS with 5+ years relevant industry experience; BS with 8+ years of relevant industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience developing, optimizing, and executing ELISA or multiplex immunoassays (MSD preferred) with demonstrated ability to troubleshoot assay performance and interpret assay data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting analytical characterization of biologic or vaccine Drug Products, ideally including materials in pre-filled syringes or vials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting bioanalytical components of product release testing and stability studies, including biochemical, biophysical, imaging, and compendial methods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with plate-based assays (Lowry, BCA, etc.), multiplexed immunoassays (MSD), microscopy methods (brightfield, scanning electron microscopy), compendial methods (osmolality, pH, etc.), and particle characterization techniques (PSD, zeta potential).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience analyzing and visualizing assay data using software tools such as Excel, Prism, or equivalent statistical/data analysis platforms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience authoring analytical technical documentation including method protocols, SOPs, reports, and study summaries, and maintaining well-documented electronic laboratory notebooks (ELN).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and the ability to manage multiple projects and shifting priorities in a dynamic development environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal and communication skills, with the ability to effectively collaborate across teams and train or mentor junior analysts when needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented with a high level of scientific rigor and excellence in data integrity and record keeping.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Scientist, Drug Product\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Onsite (minimum of 4 days per week).\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$62/hr. - $68/hr.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5213590008?gh_jid=5213590008","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":4471465008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5213590008,"updated_at":"2026-05-11T17:59:38-04:00","requisition_id":"T35-520-2026","title":"Scientist I (Contract), Protein Analytical Development","company_name":"Vaxcyte","first_published":"2026-05-11T17:59:30-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for a highly skilled, motivated, and creative analytical scientist to join Vaxcyte’s Vaccine Product Development organization as Scientist I (Contract) within Protein Development and Clinical Manufacturing. The Analytical Scientist I will assume a critical role of development and executing the key analytical methods to support the measurement of titer, impurities and product quality for in process intermediates. The successful candidate will support the set up of analytical capabilities within protein process development group, development/optimization and qualification of in process analytical methods and apply the methods for process characterization. This position is for a scientific role which will be mostly lab based, this role will require excellent scientific judgment, independence, rigor and thorough record keeping.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Method Development \u0026amp;amp; Optimization: Establish and optimize analytical methods for biologics, including HPLC (SEC, IEX/AEX), GFP assays, and protein quantification.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High-Throughput Automation: Design and implement automated workflows using liquid handling and robotic platforms (e.g., Tecan, Big Tuna) to enable high-throughput sample processing and buffer exchange.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Analysis \u0026amp;amp; Interpretation: Acquire and interpret complex data sets for lysate activity and protein characterization; provide actionable insights for process development studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Laboratory Execution: Perform precise sample preparation and plate-based assays with a focus on high accuracy and low %CV.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative Design: Partner with cross-functional SMEs to design experiments, troubleshoot instrumentation, and advance novel analytical techniques.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reporting \u0026amp;amp; Documentation: Maintain rigorous documentation in Electronic Lab Notebooks (ELNs) such as Benchling; present data-driven results at group meetings and contribute to technical reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project Ownership: Work independently to manage assigned tasks, from initial method development through to routine sample testing and troubleshooting.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: PhD with 1-2 yrs experience, or B.S in Chemistry, Analytical Chemistry, Biochemistry, or related field with minimum 8 years relevant industry experience; MS with minimum 5 years of industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Technical Proficiency: Extensive hands-on experience with AEX/SEC-HPLC ,\u0026amp;nbsp; GFP assays , and automated platforms like Big Tuna.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical Rigor: Demonstrated ability to perform reliable data analysis and interpret results within the context of process characterization and regulatory guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem Solving: Strong critical thinking skills with a proven track record of troubleshooting complex instrumentation and assay variations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Soft Skills: A proactive team player with excellent communication skills and the ability to thrive in a fast-paced, collaborative laboratory environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Innovation: A natural curiosity for applying new technologies and scientific creativity to solve complex analytical challenges.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Staff Scientist, Downstream Development for Protein Development and Manufacturing\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026lt;/strong\u0026gt; 12 months\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$62/hr.\u0026amp;nbsp; -\u0026amp;nbsp; $68/hr.\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5141938008?gh_jid=5141938008","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":4438122008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5141938008,"updated_at":"2026-05-23T11:49:44-04:00","requisition_id":"JR100072","title":"Scientist II, Conjugation Development ","company_name":"Vaxcyte","first_published":"2026-03-06T20:13:43-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for a Scientist-II, Conjugation Development. The candidate’s primary responsibility will be to lead and execute experimental activities that support company’s pneumococcal conjugate vaccine program with a focus on developing a deeper understanding of the conjugation process. In parallel, the candidate will work on conjugation process development for Vaxcyte’s pipeline programs contributing to process optimization, scalability, and technical readiness for future clinical manufacturing. Specifically, this will include preparation, purification, and analytical characterization of chemically modified polysaccharides and polysaccharide-protein conjugates. The ideal candidate will have significant laboratory experience and an excellent understanding of analytical chemistry principles. The successful candidate will be expected to design, execute, and troubleshoot experiments with minimal guidance. The candidate will also contribute when needed to a range of related areas such as analytical development and stability studies. Responsibilities will additionally include record management, data presentation at group meetings, authorship of laboratory protocols and development reports, communication with external organizations during tech transfer, and assumption of a leadership role in collaborative studies with other members of the conjugation group.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Optimize and troubleshoot multi-step syntheses of protein-polysaccharide conjugates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Purify polysaccharides and conjugates using a variety of methods including dialysis, size-exclusion chromatography, and tangential flow filtration (TFF)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze polysaccharides and conjugates with a variety of analytical methods. Develop new laboratory workflows and analyses beyond established procedures when appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advise team members on experimental design, interpretation of results, and troubleshooting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Model and train team members on best practices for adherence to protocols and data management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a subject matter expert during tech transfer of conjugation processes to contract manufacturing organizations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain highly organized records to enable optimization and assessment of reproducibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend team meetings ready to provide updates on conjugation development progress.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD in chemistry, biochemistry, or related field with minimum 2 years of industry experience, or combination of industry and postdoctoral research; MS with minimum 7 years industry experience, or BS with minimum 10 years of experience industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong biochemistry and organic chemistry knowledge base underpinning several years’ experience preparing bioconjugates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with small- and large-scale techniques for purification of bioconjugates, including tangential flow filtration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in a variety of techniques for bioconjugate analysis such as colorimetric assays, HPLC, and SEC-MALS.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sufficient knowledge of analytical principles to develop fit-for-purpose analytical methods as needed and provide cross-functional feedback on draft analytical methods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Design of Experiments is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with chemical modification of polysaccharides is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience implementing and/or using electronic notebooks is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and excellent organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills; ability to communicate effectively both verbally and in written formats.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-starter; ability to work in a fast-paced, cross-functional environment and collaborate effectively with other team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enthusiasm to learn the new skills and techniques necessary to tackle problems outside of current area of expertise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is lab based role that requires an onsite presence.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Associate Director, Conjugation Development\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$146,000 - $170,000 (SF Bay Area).\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043047008,"name":"Conjugation","child_ids":[],"parent_id":4043043008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5194792008?gh_jid=5194792008","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":4462494008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5194792008,"updated_at":"2026-06-01T15:42:03-04:00","requisition_id":"T34-520-2026","title":"Senior Associate Engineer, Upstream Development for Protein Development and Manufacturing (Contract)","company_name":"Vaxcyte","first_published":"2026-06-01T15:41:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking a talented and experienced Senior Associate Engineer to join the Upstream Process Development group within the Protein Development and CMC team. This is an exciting opportunity to join an outstanding team pursuing bacterial fermentation development at Vaxcyte.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful candidate will have the following skills and qualities:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience operating and maintaining bioreactors, including Ambr® 250, at laboratory scale.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with pilot scale fermentation and recovery equipment is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skillful in analyzing and presenting data for process improvements, troubleshooting, and optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An exceptional team player who works seamlessly with others, speaks up, and remains focused on achieving the best results to achieve company goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and planning skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and collaborate in operational activities related to bioreactor set-up, monitoring, harvest, and maintenance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, test, and implement recipe scripting for fed-batch fermentation feeding controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide engineering support for design, implementation, and qualification of scale-down models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author SOPs (standard operating procedure), process flow diagrams and batch records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze and present fermentation data at internal project meetings. Participate in upstream database management and documentation in electronic notebooks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in Chemical Engineering or a related discipline with 5+ years of relevant Pharma/Biotech industry experience, or MS with 2+ years of relevant Pharma/Biotech industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with fermentation and/or primary recovery unit operations.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Good understanding in fundamentals of bioreactor design, operation and controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of aseptic techniques\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mechanical and technical knowledge of primary recovery unit operations such as homogenization, centrifugation, and depth filtration, is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of fermentation scale up and development of scale down models\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with DoE (Design of Experiments) principles and software.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements of biotherapeutics. Late-stage process characterization experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Senior Scientist, Upstream Development for Protein Development \u0026amp;amp; Manufacturing\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;12 Months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range: \u0026lt;/strong\u0026gt;$57.00 - $63.00\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5191782008?gh_jid=5191782008","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":4461054008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5191782008,"updated_at":"2026-05-12T15:03:44-04:00","requisition_id":"T27-530-2026","title":"Senior Associate Scientist (Contract), Conjugation Development","company_name":"Vaxcyte","first_published":"2026-05-07T14:34:34-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking Senior Associate Scientist (Contract), Conjugation Development, who will support the development of a robust process for generating the company’s proprietary pneumococcal conjugate vaccine. This role will focus on analysis of vendor-supplied materials in a capacity similar to a Quality Control Lab, as well as supporting the Conjugation Development team as needed. This is lab-based, full-time position that requires strict adhesion to protocols and documentation standards. The ideal candidate has strong organizational skills, clear communication, a high level of attention to detail, and experience working in a QC environment.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Conduct analyses of vendor-supplied samples using colorimetric assays, gel electrophoresis, and liquid chromatography while strictly adhering to established SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support lab operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track shipping details for vendor-supplied samples.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review analytical assay data for adherence to SOPs and accuracy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain organized records of review status of notebook entries and analytical data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to reports, certificates, and other documentation supporting process development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate effectively with team members and contribute to cross-functional activities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS degree in Chemistry, Biochemistry, or related field with minimum 5 years of industry experience, or MS degree with minimum 3 years of industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 2 years of experience in an analytical development or quality control role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience running colorimetric assays is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with HPLC is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with SDS-PAGE is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent attention to detail, organizational skills, and record-keeping abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work both independently and collaboratively in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to integrity, professionalism, and safety in all aspects of work.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt; Scientist II, Conjugation Development\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026lt;/strong\u0026gt; 12 Months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$56/hr.\u0026amp;nbsp; $62/hr.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5154315008?gh_jid=5154315008","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":4443841008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5154315008,"updated_at":"2026-06-03T21:36:55-04:00","requisition_id":"T24-535-2026","title":"Senior Associate Scientist (Contract), Drug Product Analytics","company_name":"Vaxcyte","first_published":"2026-03-23T13:10:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, especially immunoassays and multiplexed immunoassay formats. Experience in analyzing vaccine and adjuvant-containing formulations is a plus.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In addition, Vaxcyte is looking for an experienced and flexible individual who would be comfortable working on multiple projects at once, with fluid prioritization to enable aggressive timelines. This position is for a lab-based scientific role and requires excellent scientific judgement, independence, rigor, and thorough record-keeping.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute routine and non-routine analysis of internal release, development, and stability samples using a variety of analytical techniques across Drug Product working groups, ensuring high-quality data generation and reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the execution, optimization, and continuous improvement of Vaxcyte’s internal multiplex immunoassay (MSD) assay suite, including troubleshooting assay performance, improving robustness, and supporting assay lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design, execute, and interpret experiments to support non-GxP stability studies including thermal, freeze/thaw, agitation, and container closure system evaluations for both Drug Substance and adjuvanted vaccine Drug Product materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze and interpret complex assay data, identify trends or deviations, and communicate findings to project teams to support development decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to method development, qualification, and technology transfer activities, including collaboration with external analytical laboratories and manufacturing CMOs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review technical documentation including assay protocols, SOPs, reports, study plans, and technical summaries in support of development and analytical activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Vaxcyte PCV and VAXA1 programs through cross-functional collaboration with Drug Product Development, Formulation, Analytical Development, Quality, and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Vaxcyte is seeking a flexible and collaborative Scientist comfortable managing multiple priorities in a fast-paced development environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This role is predominantly lab-based and requires strong scientific judgment, independence in experimental execution, rigor in data analysis, and meticulous record keeping.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS degree in Chemistry, Biochemistry, or related field with minimum 5 years of relevant industry experience, or MS degree with minimum 3 years of relevant industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 2 years of experience in an analytical development or quality control role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience running colorimetric assays is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with SEC-MALS is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with SDS-PAGE is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent attention to detail, organizational skills, and record-keeping abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work both independently and collaboratively in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to integrity, professionalism, and safety in all aspects of work.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Manager, Drug Product Analytics\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Onsite (minimum of 4 days per week)\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12months\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026lt;/strong\u0026gt; $56.00/hr. - $62.00/hr.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5218345008?gh_jid=5218345008","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":4473981008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5218345008,"updated_at":"2026-06-03T21:35:54-04:00","requisition_id":"T40-535-2026","title":"Senior Associate Scientist (Contract), Formulation Development","company_name":"Vaxcyte","first_published":"2026-05-13T11:24:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte has an exciting opportunity for a highly-motivated and talented individual to join our Formulation Development team. The Senior Research Associate Scientist will play a critical role in the development of innovative protein–polysaccharide conjugate vaccines.\u0026lt;br\u0026gt;The successful candidate will independently design, execute, and support formulation development activities to advance Vaxcyte’s drug product pipeline from early-stage development through clinical studies and commercialization. In this role, the candidate will lead complex experimental studies, including the design of formulation screening strategies, analytical testing, and physicochemical characterization of drug products; support investigations; and contribute to process optimization and technical problem-solving.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support and execute the manufacture of complex drug products to support formulation development, analytical development, animal immunogenicity studies, and process development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;With guidance, design, plan, and independently perform complex experiments, including troubleshooting and optimization of formulation processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze and interpret experimental data; clearly communicate findings through presentations in working group meetings and contributions to technical reports and presentations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze samples with biochemical, biophysical and particle characterization techniques, interpret results, and communicate conclusions to the broader team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare buffers, solutions, and reagents to support formulation and analytical activities, ensuring accuracy and consistency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain scientific rigor and ensure detailed, accurate documentation of all experiments conducted.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and enhance laboratory organization, including bench management, inventory control, and compliance with safety and regulatory standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure accurate, thorough, and timely documentation of all experimental work in electronic lab notebooks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position reports into the Formulation Development function and is part of the broader Process Development and Manufacturing group.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position will collaborate with cross-functional groups and the ability to work effectively in a collaborative environment is essential.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate agility in both scientific thinking and practical execution; a proactive, solution-oriented mindset is strongly encouraged.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This is a lab-based position and requires the ability to stand or sit for extended periods as well as work in biosafety cabinets.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS degree in Chemistry, Biochemistry, or related field with minimum 5 years of relevant industry experience, or MS degree with minimum 3 years of relevant industry experience. Experience in vaccine formulation development is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong hands-on experience in buffer preparation, formulation development, and laboratory techniques.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to independently design and execute experiments and troubleshoot technical challenges.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in maintaining detailed and accurate records; experience with electronic lab notebooks (ELN) is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience interpreting complex data sets with data analysis tools (e.g., GraphPad Prism, JMP) and a solid understanding of statistical analysis is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills with attention to detail in pipetting, sample preparation, and data recording.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Office (Word, Excel, PowerPoint).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to work effectively in a cross-functional, collaborative environment across multiple projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, written, and verbal communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated initiative, scientific curiosity, and the ability to contribute strategically within a fast-paced team.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Scientist II, Formulation Development\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Onsite (minimum of 4 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length: \u0026lt;/strong\u0026gt;12months\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$56/hr.- $62/hr.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/4671584008?gh_jid=4671584008","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":4235197008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":4671584008,"updated_at":"2026-04-14T11:31:06-04:00","requisition_id":"T22-525-2026","title":"Senior Associate Scientist (Contract), Polysaccharide Analytical Development","company_name":"Vaxcyte","first_published":"2026-03-17T12:29:49-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated and detail-oriented Senior Associate Scientist (Contract) to join our Polysaccharide team. Primary responsibility for the incumbent will be to support analytical testing and characterization of polysaccharide-based drug candidates. This individual will execute and optimize a variety of biochemical and chromatographic assays, contribute to method development initiatives, and ensure high-quality data generation in support of research and development programs. \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role requires strong hands-on experience in HPLC-based techniques, biochemical assays, and analytical software platforms, along with a commitment to data integrity, documentation excellence, and cross-functional collaboration.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Essential Functions:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Analytical Testing \u0026amp;amp; Characterization\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform in-house assays for polysaccharide manufacturing, including in-process testing, process development and process characterization study sample analysis, including:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;HPLC-based assays (e.g., HPLC-RI, HPAEC-PAD, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Spectrophotometric-based assays (e.g., UV/Vis, Lowry, PicoGreen, Anthrone, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enzyme- and/or Immuno assays (e.g., ELISA, MSD platforms)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Nephelometry (e.g. Turbidity analysis)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Metabolite Analysis (e.g. sugars)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;LC-MS-based assay\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Prepare samples, reagents, standards, and controls according to established protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot instrumentation and assay performance issues to ensure reliable data output.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Method Development \u0026amp;amp; Optimization\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist in developing, qualifying, and optimizing analytical methods for sample preparation, testing, and characterization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support method transfer, robustness evaluation, and documentation updates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively recommend improvements to increase assay sensitivity, reproducibility, and throughput.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Data Analysis \u0026amp;amp; Reporting\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Utilize data analysis software platforms such as Empower and Chromeleon for HPLC data acquisition and analysis, and SoftMax Pro for MSD and spectrophotometric assay data analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze, interpret, and summarize experimental data clearly and concisely.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare technical summaries and present findings to cross-functional teams (e.g., R\u0026amp;amp;D, CMC, Quality).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Compliance \u0026amp;amp; Documentation\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain meticulous laboratory notebooks and electronic records in compliance with internal SOPs and laboratory standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure data integrity and adherence to applicable regulatory guidelines (e.g., GLP/GMP where applicable).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in audits, documentation reviews, and quality initiatives as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Collaboration \u0026amp;amp; Continuous Learning\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate effectively with scientists across disciplines to support program milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate eagerness to learn new analytical techniques and scientific concepts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Integrate best laboratory practices and contribute to a culture of operational excellence.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MSc in Chemistry/Biochemistry, Biotechnology, or similar degree with a minimum of 3 years of relevant industry experience, or BSc with a minimum of 5 years of relevant industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with HPLC systems and carbohydrate or polysaccharide analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with HPAEC-PAD is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with LC-MS/MS is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Empower and/or Chromeleon software.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with biochemical assays (ELISA, colorimetric, fluorescence-based assays).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with polysaccharides, biologics, or complex drug substances.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in in-process monitoring and testing for process-related impurities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of regulatory expectations for analytical documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting CMC, process development, or analytical development programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to data accuracy and reproducibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative team player with proactive communication style.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuous improvement mindset.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt; Senior Scientist, Polysaccharide Analytical Development\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; San Carlos, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;12months\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hourly Range:\u0026lt;/strong\u0026gt; $56.00/hr. - $62.00/hr.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/4816461008?gh_jid=4816461008","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":4299150008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Temporary","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":4816461008,"updated_at":"2026-05-18T19:45:06-04:00","requisition_id":"T23-525-2026","title":"Senior Associate Scientist (Contract), Upstream Polysaccharide Process Development","company_name":"Vaxcyte","first_published":"2025-07-22T19:39:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Development organization is comprised of four Process teams: Protein, Polysaccharide, Conjugate Drug Substance (Conjugation), and Drug Product. These Process Development teams are supported by Analytical Development and Formulation Development teams. Vaxcyte is looking for a Senior Associate Scientist (contract) with experience in microbial fermentation and upstream processing to join the Upstream Polysaccharide Process Development team. The candidate will be responsible for collaboration on experimental design and execution of experiments to further develop and optimize upstream processes for polysaccharide manufacturing using microorganisms. The successful candidate will have practical laboratory experience related to microbial fermentation processes and eager to utilize and learn new laboratory skills. The role will require \u0026amp;gt;50% time in the lab and this person will be able to independently detail experimental procedures/results in written and presentation formats. The successful candidate may interface closely with the cross-functional team, write detailed technical reports, present experimental results internally, and may potentially interface with external CMO partners.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support in study design, execute, and analyze experiments for upstream polysaccharide for bacterial fermentation (BSL2) and vaccine production processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute experiments to develop the upstream process parameters (e.g., media, feed, pH, temperature, dissolved oxygen, agitation, etc.) and to enhance product yield, quality, and consistency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform microbiology related work including plating, colony selection, Gram staining and cell enumeration on microscope.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform fermentation vessel assembly and script writing for process automation and execute fermentation experiment in shake-flask and lab scale bioreactors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare media and buffer as needed for experiments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operate and maintain instrumentation for bacterial fermentation and primary recovery (centrifugation, filtration, etc.) of bacterial polysaccharides utilizing aseptic techniques.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support analytical method execution including optical density, residual metabolites and polysaccharide concentration and other relevant analytical techniques.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in executing process development studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Keep accurate and current records of research and/or project related activities in laboratory notebooks and Electronic Lab Notebook.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and review protocol, technical reports, SOPs, and batch records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present and communicate scientific data and results to internal stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be an outstanding teammate and collaborate effectively with cross functional team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;and collaborate effectively with downstream, analytical, and manufacturing teams within Polysaccharide Development and Manufacturing team to ensure seamless technology transfer and process integration.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MSc in Chemical/Biochemical Engineering, Biotechnology, or similar degree with a minimum of 3 years of relevant industry experience, or BSc with a minimum of 5 years of relevant industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in handling microorganisms with proper aseptic techniques to perform upstream processing related work in flasks/bioreactors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience and theoretical understanding of key processing operations such as microbial culture, fermentation process, microbial media, and process optimization and relevant analytical technologies; experience with depth filtration, continuous centrifugation is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and optimize scripts for instrumentation, including Ambr® systems, to enhance efficiency and automate processes, leveraging programming languages such as Python or R is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Design of Experiments (DoE) principles and DoE software.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process characterization experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cell banking expertise, colony selection and genetic analysis of recombinant strains is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with computer programs such as Microsoft Excel, Word, PowerPoint, Visio and JMP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of GMP requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to succeed in a cross-functional team environment, effectively managing multiple projects and contributing to team outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills, with excellent written and verbal communication abilities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Scientist, Upstream Polysaccharide Process Development\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Expected Contract Length:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;12months\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Hourly Range: \u0026lt;/strong\u0026gt;$56.00/hr. - $62.00/hr.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4063013008,"name":"Temporary Opportunities","child_ids":[],"parent_id":null}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5142485008?gh_jid=5142485008","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":4438382008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5142485008,"updated_at":"2026-05-18T14:29:55-04:00","requisition_id":"728-920-2026","title":"Senior Azure Cloud Engineer","company_name":"Vaxcyte","first_published":"2026-03-13T11:31:39-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a skilled and passionate Azure Cloud Engineer to join our growing engineering team. In this role, you will design, build, and maintain secure, scalable cloud infrastructure on Microsoft Azure, using Infrastructure as Code (IaC) best practices — primarily Terraform. You will collaborate with cross-functional teams to deliver reliable hosting solutions that meet the highest standards of security and compliance.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate holds an Azure certification, brings strong software engineering fundamentals, and has hands-on experience with a broad range of Azure services. Experience in validated or regulated environments, particularly within the Life Sciences sector, is considered a valuable plus.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Infrastructure \u0026amp;amp; Cloud Engineering\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design, deploy, and manage Azure cloud infrastructure using \u0026lt;strong\u0026gt;Terraform\u0026lt;/strong\u0026gt; and Infrastructure as Code (IaC) best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provision and maintain Azure services including \u0026lt;strong\u0026gt;AKS, ADF, Microsoft Fabric, Managed SQL Instances, Virtual Machines,\u0026lt;/strong\u0026gt; and \u0026lt;strong\u0026gt;Batch Accounts.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain secure virtual networks, including firewalls, private endpoints, NSGs, and network segmentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure infrastructure meets organizational security standards, including identity and access management via \u0026lt;strong\u0026gt;Azure AD / Entra ID\u0026lt;/strong\u0026gt; and RBAC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Configure and monitor logs and notifications to proactively identify issues and minimize downtime.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor Azure end of support components and plan changes and updates to the infrastructure as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, test and maintain backup and disaster recovery plans for infrastructure.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Security \u0026amp;amp; Compliance\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Enforce security controls and conduct regular audits to maintain compliance with organizational and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support validated and regulated environmental requirements (e.g. GxP, ISO, SOC 2) where applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor infrastructure health and respond to security incidents promptly and effectively.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Collaboration \u0026amp;amp; Continuous Improvement\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with software, data engineering, and platform teams to support application hosting and CI/CD pipelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document architecture decisions, runbooks, and operational procedures to support team knowledge sharing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and adopt new Azure services and cloud-native tooling to improve platform reliability and efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to monitoring, logging, and observability improvements across the infrastructure estate.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Bachelor’s degree in computer science, Engineering, or related field (or equivalent experience) with a minimum of 5+ years of experience. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Microsoft Azure certification (e.g. AZ-104, AZ-305, or equivalent) is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience with \u0026lt;strong\u0026gt;Terraform\u0026lt;/strong\u0026gt; for provisioning and managing cloud infrastructure at scale.Strong understanding of Azure networking: VNets, subnets, NSGs, private DNS, and firewall configurations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with Azure services: \u0026lt;strong\u0026gt;AKS, ADF, Managed SQL, VMs,\u0026lt;/strong\u0026gt; and \u0026lt;strong\u0026gt;Batch Accounts.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid software engineering fundamentals: version control (Git), scripting (PowerShell/Bash/Python), and code review practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience implementing cloud security controls, including identity management and RBAC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills with the ability to explain technical concepts to varied audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong architectural and systems design capability with an infrastructure-as-code mindset.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ownership mindset with accountability for reliability, security, and performance outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to automation, documentation, and operational excellence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance technical rigor with delivery timelines in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative team player who works effectively across engineering and business functions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience working in validated or regulated environments (e.g. GxP, ISO, SOC 2).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in the Life Sciences, Pharmaceutical, or Healthcare sectors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with \u0026lt;strong\u0026gt;Microsoft Fabric\u0026lt;/strong\u0026gt; and modern data platform architectures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of DevOps and GitOps workflows, including Azure DevOps or GitHub Actions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with cloud cost optimization strategies and governance frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Associate Director, Data Systems, CMC IT\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement:\u0026lt;/strong\u0026gt; Hybrid (minimum of 2-3 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$163,000 - $191,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043035008,"name":"IT","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5165575008?gh_jid=5165575008","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":4449287008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5165575008,"updated_at":"2026-05-18T13:21:03-04:00","requisition_id":"729-920-2026","title":"Senior Computer Systems Validation Engineer","company_name":"Vaxcyte","first_published":"2026-03-26T13:16:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Senior Computer Systems Validation (CSV) Engineer is responsible for leading validation activities for cloud based GxP systems to ensure they meet regulatory, quality, and operational requirements throughout the system lifecycle. The role focuses on traditional Computer System Validation with application of risk-based Computer Software Assurance (CSA) principles where appropriate.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The individual will work closely with IT and Quality teams to validate and maintain GxP systems across their lifecycle. Strong experience validating relational databases, cloud infrastructure, and integrated applications in regulated biotech or pharmaceutical environments is required.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a hands-on role requiring authoring and executing validation documents and protocols for GAMP 5 systems.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a hybrid role with minimum of 3 days a week onsite at San Carlos, CA location.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Hands-on lead full lifecycle Computer System Validation activities for cloud based GxP systems including databases, and applications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author, update, execute and maintain validation deliverables such as Validation Plans, User Requirements, Functional Specifications, Risk Assessments, Traceability Matrices, IQ, OQ, PQ protocols, and Summary Reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform risk assessments to define validation scope, testing strategy, and documentation requirements in alignment with CSA principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and execute validation strategies for data platforms and system components, ensuring systems meet defined functional, security, and data integrity requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess and validate end to end data flows between upstream source systems and downstream applications to ensure accuracy, completeness, and traceability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate system changes for validation impact and ensure validated systems remain compliant through appropriate testing and documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure validation activities align with automated build and deployment pipelines, confirming that system releases maintain validated state and appropriate validation evidence is generated.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support change control, deviation management, periodic review, and lifecycle management of validated systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in internal audits and regulatory inspections, providing validation documentation and rationale as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to continuous improvement of validation procedures aligned with evolving CSA guidance and cloud delivery models.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Computer Science, Engineering, Life Sciences, or related field, or equivalent professional experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 7 years of experience in Computer System Validation within biotech manufacturing and lab data systems. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must have technical knowledge of IT infrastructure, software engineering, programming, databases and data integrations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in modern system environments utilizing CI/CD pipelines or automated release processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong hands-on experience validating GAMP 5 systems for biotech manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of FDA 21 CFR Part 11, Part 210, Part 211, Annex 11, data integrity requirements, and risk-based validation methodologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong technical writing skills and ability to create comprehensive validation documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate validation risks and requirements clearly to IT and Quality stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Other combinations of education and/or experience may be considered.\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026lt;/strong\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience validating cloud based GxP systems, specifically Azure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with infrastructure as code frameworks like GitHub, Terraform etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience applying CSA principles to custom data applications in GxP cloud.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Microsoft Azure or similar technical certifications.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Manager, Data Systems\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Hybrid (minimum of 3 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$164,000 - $190,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is not eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043035008,"name":"IT","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/4918256008?gh_jid=4918256008","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":4338515008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":4918256008,"updated_at":"2026-05-18T13:22:36-04:00","requisition_id":"598-340-2025","title":"Senior Director, Global Logistics and Distribution","company_name":"Vaxcyte","first_published":"2025-10-03T19:20:12-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Global Logistics \u0026amp;amp; Distribution has overall responsibility for shipping and storage of all Vaxcyte CMC materials including finished goods, bulk product and samples. Scope includes material for Research, Development, Clinical and Commercial. This position will report to the Executive Director, Global Supply Chain.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;STRATEGIC PLANNING:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement a global logistics and distribution strategy aligned with corporate objectives including network design, transportation optimization and warehousing operations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;OPERATIONS MANAGEMENT:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure the efficient, timely, compliant and high-quality delivery of all materials in scope\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that pack-outs are robustly designed with the appropriate containers and associated components to maintain material at target temperature and facilitate efficient receipt\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure robust shipping agreements are in place with CMOs and suppliers of criterial raw materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversight of all logistics related policies, guidelines, SOPs and Work Instructions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure sound inventory management practices are in place at all storage facilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure inventory losses are minimized to lowest possible levels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and track Key Performance Indicators\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;COMPLIANCE / REGULATORY:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with international trade laws, import/export regulations, tariffs and customs requirements, including managing country of origin, customs valuation and documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all shipping and storage operations are compliant with Good Distribution Practices (GDP)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that temperature excursions and other logistics related deviations occur at low frequency and are resolved in a compliant and timely manner with minimal material losses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure external supply chain partners have an established CAPA program and monitor the same\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the successful design \u0026amp;amp; execution of a Shipping Validation Program\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;VENDOR MANAGEMENT:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Select and Manage relationships with logistics providers, transportation companies, freight forwarders, third-party logistics (3PL) partners, import /export brokers and other logistics service providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Select and manage relationships with passive and active cold chain packaging/container vendors\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;RISK MANGEMENT:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Identify and mitigate risks within the logistics network to ensure product supply continuity\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;TEAM LEADERSHIP:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead, mentor, and scale a high-performing global logistics team, fostering a culture of continuous improvement and professional development.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;FINANCIAL OVERSIGHT:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage the global logistics budget, conduct financial analyses to support decision-making, and ensure cost-effectiveness without compromising quality or service.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure tariff obligations are managed in a cost-effective manner.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;TECHNOLOGY \u0026amp;amp; AUTOMATION:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Drive the adoption of advanced technologies and automation within logistics operations to enhance efficiency and resilience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Development and maintenance of IT systems to track shipping requests, actual shipments and temperature data.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;CROSS FUNCTIONAL COLLABORATION:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Interface with Vaxcyte Commercial, Quality, Finance, IT, Process Development, Regulatory, Legal MSAT, Supply Planning, Clinical Supply, Supplier Management, Project Management, Operations and other Functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interface with Logistics staff at CMOs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS in a science-related discipline is a definite plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12+ years’ experience working in the Life Sciences industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12+ years’ experience in International cGMP cold chain shipping\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a pharmaceutical 3PL\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fluent with all global shipping-related statutory and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand the requirements, technologies, and processes of cold-chain supply management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with pharma logistic service providers with knowledge of qualified active and passive containers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with arranging international and domestic transportation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience authoring and using GxP documents such as SOP’s and work instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relentless focus and passion around process improvements (efficiency and automation).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, customer service, and relationship skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Vaccine distribution experience highly valued.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Vice President, Global Supply Chain\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Hybrid (minimum of 3 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$260,000 – $303,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4046547008,"name":"Global Supply Chain","child_ids":[],"parent_id":4043054008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5071525008?gh_jid=5071525008","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":4404265008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Remote","value_type":"single_select"}],"id":5071525008,"updated_at":"2026-06-02T00:30:04-04:00","requisition_id":"732-870-2026B","title":"Senior Director, Product Launch Lead VAX-31","company_name":"Vaxcyte","first_published":"2026-01-20T13:32:09-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking a Senior Director, Launch Lead, VAX-31, to lead strategic planning and execution of the company’s first launch of VAX-31. This role will coordinate cross-functional activities from late-stage development through market entry, ensuring readiness across supply chain, regulatory, medical affairs, commercial operations, communications, and other functions. The position will partner with senior leadership to define launch strategies, manage timelines, mitigate risks, and drive alignment across internal and external stakeholders to deliver successful product introductions globally.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Drive cross functional launch delivery of VAX-31 and oversee integrated launch plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment with corporate objectives and market requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain comprehensive launch readiness frameworks, including working with supply chain, manufacturing scale-up, regulatory approvals, labelling, distribution, and commercial execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Commercial, Medical Affairs, Regulatory, Quality, Manufacturing, Finance, Market Access, and Scientific Affairs teams to ensure seamless coordination and timely decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate cross-functional launch meetings, track critical milestones, and proactively identify risks and contingency plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive post-launch performance tracking and lessons learned to inform future launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion best practices in pharmaceutical launch project management, including governance models, risk registers, and stakeholder engagement strategies.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS in life sciences, engineering, or business; advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 15 years in pharmaceutical or biotechnology industry, with at least 5 years in launch related project management or product marketing/management; vaccine launch experience strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure adherence to project scope, budget, and schedule; ensure the alignment of the project to corporate strategic direction, resource allocation, and management decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate team meetings, cross-functional communication, and decision-making; ensure alignment with internal and external stakeholders, program and project teams and functional area partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support continuous improvement efforts in Project Management practices at Vaxcyte.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of leading successful product launches in multiple markets. Expertise in cross-functional leadership, strategic planning, and risk management for complex launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of regulatory pathways, supply chain logistics, and market access considerations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough understanding of product development activities in biotech/drug/vaccine development, including key interdependencies, and knowledge of proven development strategies and tactics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated strong organizational and strategic leadership skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated aptitude for successfully managing multiple projects, of varying complexity, within the specified guidelines, timeframes, and budgets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-starter with the ability to work independently, deal with ambiguity, and execute.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert planning and tracking skills, well-organized, focused on results, capable of managing multiple projects with respect to priorities and self-management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven influence management and communication skills, at all levels of the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert knowledge of MS Word, Excel, PowerPoint, Visio, and Project.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and oral communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Chief Commercial Officer\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;East Coast - US\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement: \u0026lt;/strong\u0026gt;Remote\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$271,000 - $316,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043039008,"name":"Commercial","child_ids":[4070438008],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null},{"id":4060325008,"name":"US - Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5045875008?gh_jid=5045875008","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":4392953008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5045875008,"updated_at":"2026-03-18T15:58:47-04:00","requisition_id":"JR100026","title":"Senior IT Business Systems Analyst, SAP Finance","company_name":"Vaxcyte","first_published":"2026-01-07T14:50:01-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span class=\u0026quot;TextRun SCXW253599438 BCX0\u0026quot; lang=\u0026quot;EN-US\u0026quot; data-contrast=\u0026quot;auto\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;Vaxcyte is undergoing a major ERP transformation, moving from NetSuite to SAP S/4HANA to support its rapid growth\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;and upcoming transition to commercial operations.\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;\u0026amp;nbsp;The\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;Senior\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;IT\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;Business\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;Systems\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;Analyst (BSA),\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;SAP\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;F\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;inance\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;\u0026amp;nbsp;will play a critical role in bridging Finance and IT, ensuring a smooth transition and successful implementation of SAP S/4HANA Finance modules. This position requires strong functional\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;expertise\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;NormalTextRun SCXW253599438 BCX0\u0026quot;\u0026gt;\u0026amp;nbsp;in SAP Finance, deep understanding of accounting processes, and experience in ERP migration projects.\u0026lt;/span\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;EOP SCXW253599438 BCX0\u0026quot; data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:200,\u0026amp;quot;335559739\u0026amp;quot;:0,\u0026amp;quot;335559740\u0026amp;quot;:276}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li style=\u0026quot;line-height: 1;\u0026quot; data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Support the migration from\u0026amp;nbsp;NetSuite to SAP S/4HANA, ensuring data integrity and process continuity.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;2\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Collaborate with Finance and IT teams to design future-state processes aligned with\u0026amp;nbsp;Vaxcyte’s\u0026amp;nbsp;business needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; 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data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;5\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Configure and\u0026amp;nbsp;maintain\u0026amp;nbsp;SAP Finance modules\u0026amp;nbsp;including Financial Accounting (FI), Controlling (CO), Treasury \u0026amp;amp; Cash Management, Financial Close \u0026amp;amp; Reporting, and Procurement.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;6\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Work closely with Finance stakeholders (Accounting, FP\u0026amp;amp;A,\u0026amp;nbsp;Procurement) to capture requirements.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;7\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Translate business needs into functional specifications for SAP configuration.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;8\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Help develop and document business process flows.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;9\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Develop and execute test plans for SAP Finance processes.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;10\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Support\u0026amp;nbsp;User Acceptance Testing (UAT)\u0026amp;nbsp;and resolve issues promptly.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;11\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Create training materials and deliver sessions for Finance users transitioning from NetSuite.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;12\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Provide ongoing support\u0026amp;nbsp;post go-live.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;31\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;13\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Ensure compliance with GAAP and biotech industry standards.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li style=\u0026quot;line-height: 1;\u0026quot; data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;35\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Minimum 7\u0026amp;nbsp;years of experience\u0026amp;nbsp;as a BSA with SAP Finance modules.\u0026amp;nbsp;Other combinations of education and/or experience may be considered.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;35\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;2\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Bachelor’s degree in\u0026amp;nbsp;Finance, Accounting, Information Systems, or related field.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;35\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;3\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Strong analytical and problem-solving skills, with the ability to\u0026amp;nbsp;identify\u0026amp;nbsp;issues and implement effective solutions.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;35\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;4\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience in\u0026amp;nbsp;identifying\u0026amp;nbsp;and managing project risks, with a proactive approach to mitigation.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;35\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;5\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;\u0026amp;nbsp;Familiarity with\u0026amp;nbsp;change management principles and techniques to\u0026amp;nbsp;facilitate\u0026amp;nbsp;smooth transitions and adoption of new systems.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Hands-on experience with\u0026amp;nbsp;SAP S/4HANA Finance\u0026amp;nbsp;(implementation or migration projects preferred)\u0026amp;nbsp;and Fiori applications.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;2\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience with\u0026amp;nbsp;Netsuite\u0026amp;nbsp;preferred.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;3\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience developing and mapping business process flows using Visio or similar tool\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;4\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Strong understanding of\u0026amp;nbsp;financial processes\u0026amp;nbsp;and ERP migration best practices.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;5\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Excellent communication and stakeholder management skills.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;6\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;SAP certification in FI/CO\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;7\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Expertise\u0026amp;nbsp;with agile\u0026amp;nbsp;methodology, global deployments, and data migration planning.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;8\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Experience working in\u0026amp;nbsp;GxP\u0026amp;nbsp;validated and SOX regulated systems\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;9\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Knowledge of\u0026amp;nbsp;integrated tools\u0026amp;nbsp;(e.g.,\u0026amp;nbsp;BlackLine, Concur, Ariba) and reporting solutions.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li style=\u0026quot;line-height: 1;\u0026quot; data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;33\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;multilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;10\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Other combinations of education and/or experience may be considered.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Director, IT Finance Systems\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$163,000 - $190,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043035008,"name":"IT","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5095641008?gh_jid=5095641008","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":4415869008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5095641008,"updated_at":"2026-05-01T16:33:31-04:00","requisition_id":"JR100041","title":"Senior IT Business Systems Analyst, SAP Supply Chain","company_name":"Vaxcyte","first_published":"2026-01-27T11:44:14-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is undergoing a major ERP transformation, moving to SAP S/4HANA to support its rapid growth and upcoming transition to Commercial Operations. The IT SAP Supply Chain Senior Business Systems Analyst (BSA) will play a critical role in bridging Supply Chain and IT, ensuring successful implementation, stabilization, and ongoing optimization of SAP S/4HANA Supply Chain capabilities. This position requires strong functional expertise in SAP Supply Chain functionalities, deep understanding of contract manufacturing processes, and experience in complex ERP implementation projects.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the implementation and stabilization of SAP S/4HANA Supply Chain modules in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Supply Chain, Manufacturing, Quality, and IT teams to design future-state processes aligned with Vaxcyte\u0026#39;s CDMO business model.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in data mapping, migration, cleansing, and validation during cutover and post-go-live activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth knowledge of SAP S/4HANA systems and integration techniques with third-party planning systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise with agile methodology, global deployments, and data migration planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in GxP validated and SOX regulated systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Configure and maintain SAP Supply Chain modules including Materials Management (MM), Master Data, Subcontracting \u0026amp;amp; External Processing, Batch Management, and Forecast Consumption \u0026amp;amp; Demand Planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with the integration points with FI (Financial Accounting) \u0026amp;amp; CO (Controlling)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support end-to-end planning flows from demand through manufacturing and supply execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills, with the ability to effectively communicate complex technical concepts to non-technical stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with Supply Chain stakeholders (Planning, Procurement, Finance) to capture requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate business needs into functional specifications for SAP configuration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help develop and document business process flows.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support complex planning scenarios where capacity, lead times, and execution are controlled by external CDMO partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute test plans for SAP Supply Planning processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support User Acceptance Testing (UAT) and resolve issues promptly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure validation readiness and maintain audit trail expectations in compliance with regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Training \u0026amp;amp; Change Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create training materials and deliver sessions for Supply Chain users.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing support post go-live.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with GxP standards and Life Sciences industry requirements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 7 years of experience as a BSA with SAP Supply Chain modules.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in Supply Chain, Operations, Information Systems, or related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills, with the ability to independently diagnose and resolve SAP supply chain issues in complex CDMO-based manufacturing environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in identifying and managing project risks, with a proactive approach to mitigation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with change management principles and techniques to facilitate smooth transitions and adoption of new systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with SAP S/4HANA Supply Chain (implementation or migration projects preferred) and Fiori applications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience supporting SAP-based contract manufacturing or CDMO operating models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing and mapping business process flows using Visio or similar tool.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of Supply Chain processes and ERP implementation best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and stakeholder management skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid experience managing SAP master data relevant to supply planning (materials, vendors, sourcing, BOMs).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt; Director, IT Supply Chain Systems\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$163,000 - $190,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043035008,"name":"IT","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5215113008?gh_jid=5215113008","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":4472277008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5215113008,"updated_at":"2026-05-11T11:46:07-04:00","requisition_id":"718-920-2026","title":"Senior IT Systems Analyst, G\u0026A","company_name":"Vaxcyte","first_published":"2026-05-11T11:46:07-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Sr. IT Systems Analyst, G\u0026amp;amp;A is responsible for leading the architecture, design, and evolution of G\u0026amp;amp;A platforms, with a strong focus on scalable process design and cross-system integration. This role partners with HR, IT and other G\u0026amp;amp;A teams to implement and support end-to-end business processes, establish architectural standards, and contribute to technology decisions that enable efficiency and growth. The analyst ensures platform reliability, data integrity, and seamless operations while delivering strategic enhancements and managing system releases in alignment with organizational priorities. This is a hands-on role that reports to the Associate Director of Enterprise IT Systems at Vaxcyte’s San Carlos, California headquarters.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as an IT point of contact for G\u0026amp;amp;A stakeholders; gather, analyze, and document business needs for processes and systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document current-state and future-state processes; translate business needs into functional requirements, and system specifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support governance and compliance controls (e.g., SOX ITGC where applicable), including access reviews, role/permission audits, segregation of duties considerations, and evidence documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support recurring reporting cycles and audit requests by ensuring data quality, traceability, and timely delivery of requested information.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive SDLC standards and best practices for technology delivery (intake, requirements, design, testing, release, and documentation) to improve consistency, quality, and auditability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate communication between HR, IT, other G\u0026amp;amp;A teams and implementation partners to align on scope, priorities, timelines, and outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support implementation of new features and releases, including test planning, test script creation, UAT coordination, regression testing, rollout planning, and post-go-live stabilization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain support materials, training content, job aids, and end-user documentation to drive adoption and consistent process execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure G\u0026amp;amp;A systems are operated in accordance with IT policies and procedures, privacy/security expectations, and applicable regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage governance for change management across the responsible G\u0026amp;amp;A ecosystem (e.g., change intake and prioritization, change calendar, risk/impact assessment, approvals/CAB as applicable, communications, and release readiness).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain documentation (requirements, process flows, training, end-user guides) and deliver enablement as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in computer science, information systems, or related field. Minimum 7 years of experience supporting enterprise applications, including HR systems (Workday), contingent workforce management solutions,\u0026amp;nbsp;and other G\u0026amp;amp;A systems. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with integrations (e.g., API-based integrations, SFTP/file-based interfaces, data mapping/transformations, monitoring, error handling, and reconciliation).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong data analysis skills: ability to validate data, reconcile results, and perform basic queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of SDLC practices and IT controls (ITGC), including security and compliance expectations; experience supporting SOX controls and audit evidence collection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical, troubleshooting, and problem-solving skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Business process mapping experience (current-state/future-state), including documenting end-to-end processes and identifying control points.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to translate complex business needs into clear functional requirements and technical-ready specifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and stakeholder management skills; able to translate between business and technical teams and produce clear documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfort working in a fast-paced, evolving environment with cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly motivated, results-focused, and able to manage multiple priorities with a sense of urgency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with GxP validated systems, supporting CSA/validation documentation, change control, deviation/CAPA support, and inspection/audit readiness is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Life Sciences industry experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Associate Director, IT Enterprise Systems\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA; Ability to be onsite 2 to 3 days a week.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$164,000 – $191,000\u0026amp;nbsp;(SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043035008,"name":"IT","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5195377008?gh_jid=5195377008","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":4462820008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5195377008,"updated_at":"2026-04-22T14:59:33-04:00","requisition_id":"742-820-B","title":"Senior Manager, Indirect Procurement - Clinical","company_name":"Vaxcyte","first_published":"2026-04-22T14:59:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;This is an exciting opportunity to lead procurement support for clinical development programs, serving as a strategic business partner to the Clinical Operations Department, while maintaining the ability to flex across enterprise-wide procurement priorities as business needs evolve.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role sits within the centralized Procurement function in Finance and serves as the primary procurement business partner to the Clinical organization. The Senior Manager, Indirect Procurement - Clinical will lead and support end-to-end procurement activities for clinical trials—from study start-up through closeout—while also flexing across other indirect spend categories to support broader enterprise needs. This role partners closely with Clinical Operations, Finance, and Legal to ensure timely, compliant, and cost-effective execution of vendor engagements.\u0026lt;strong\u0026gt;\u0026amp;nbsp; \u0026lt;/strong\u0026gt;Procurement owns activities including, but not limited to, the requisition to PO lifecycle, vendor selection support, contracting coordination, spend visibility/controls.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary procurement business partner to Clinical stakeholders, providing guidance and influencing vendor strategy, budgeting, and procurement processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and manage the end-to-end requisition-to-purchase order process, ensuring compliance with procurement policies and timely processing of purchasing requests.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the request for proposal process including bid comparison, bid review meetings, recommendation on selection and awarding the service.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide procurement support across additional indirect spend categories (e.g., professional services, G\u0026amp;amp;A, IT) as business needs evolve.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Finance to support budgeting, forecasting, accruals, and spend tracking for clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive standardization and continuous improvement of procurement processes, templates, and workflows in partnership with Finance and Procurement leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Support contract negotiation activities in partnership with Clinical Operations and Legal, contributing procurement expertise to ensure appropriate terms, risk mitigation, and alignment with company policies, while ensuring purchase order readiness and alignment with procurement processes prior to contract execution.\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage multiple concurrent procurement activities across clinical programs and other categories in a fast-paced, evolving environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Bachelor’s Degree in Business Administration or related field, with a minimum of 8+ years of procurement, sourcing, or vendor management experience, including experience supporting clinical trials or clinical services in a biopharmaceutical or CRO environment preferred. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting Phase I–III clinical trials, including large, multi-site studies with significant patient enrollment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must possess strong analytical ability, and solid business acumen including an understanding of business operations in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently, prioritize work, and handle simultaneous assignments under tight deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with procurement and financial systems (e.g., Netsuite, SAP, Coupa, Ariba, Oracle) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced knowledge of Excel, PowerPoint and Word are required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work collaboratively across organizations and utilize resources effectively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in the HQ office 3-5 days a week\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Executive Director, Procurement\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$159,000 - $186,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043031008,"name":"Accounting \u0026 Finance","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5222251008?gh_jid=5222251008","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":4475669008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Remote","value_type":"single_select"}],"id":5222251008,"updated_at":"2026-05-26T14:38:00-04:00","requisition_id":"654-515-2026","title":"Senior Manager, Microbiology Support for Global ASAT","company_name":"Vaxcyte","first_published":"2026-05-21T12:06:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for an energetic and talented individual to join our Analytical Science and Technology (ASAT) as a Sr. Manager. The position will be an integral part of the team responsible for cGMP-compliance in routine operations for all phases of clinical development for Vaxcyte’s PCV product to commercialization. The primary responsibility will include supporting the microbiological quality control activities including cGMP analytical testing at Contract Testing Organizations and Vaxcyte QC laboratory operations. The ideal candidate will apply technical expertise, strong cGMP experience, ensure compliant operations and documentation, foster open communication, and pursue data-driven approaches. The ideal candidate will have expertise in microbiological assays (bioburden, endotoxin, sterility and culture purity) as well as understanding or experience with aseptic manufacturing (EM, smoke studies, media fills, etc.).\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the technical expert for QC microbiological assays.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the authoring and review internal SOPs related to microbial Quality Control policies and procedures. Also support the authoring of BLA sections as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for quality event management (deviations, investigations, change control) related to microbiology QC and aseptic manufacturing operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage outsourced cGMP and characterization testing supporting lot release.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Analytical Development, Quality Control, and Product Development (and MSAT) and interface with key stake holders to understand methods being performed onsite and at CMOs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply technical and compliance expertise to the review of test methods and in-process/release documentation and provide technical and compliance feedback to internal and external stakeholders who have developed/verified the microbiological methods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with others to identify opportunities for continuous improvement and implement/maintain solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strong teamwork in establishing a quality culture and shared accountability.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Degree(s) in Microbiology, Biology, Biochemistry, or related discipline with a minimum of 7+ years of relevant experience for Ph.D., 9+ years for M.S./M.A., or 11+ years for B.S./B.A. Other combinations of education and/or experience may be considered. 7+ years of experience in Pharma / Biotech industry in aseptic manufacturing or microbiology required. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of various analytical methodology principles and experience with GMP release testing. Knowledge of microbial control methods (e.g. Bioburden, Endotoxin, Sterility, Growth Promotion).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience in analytical method verification, development, validation and transfer is highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced leading investigations into microbiological non-conformances (deviations, out-of-specification results), writing and approving Exception Reports (ERs), and driving CAPA (Corrective and Preventive Actions) implementation; displaying excellent organization, problem solving, and strategic planning skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of relevant cGMPs, FDA, EU, and ICH regulatory guidelines as applicable to QC operations/aseptic processing/manufacturing sterility assurance, and/or compendial methods (USP/EP/JP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to apply the knowledge and understand/gain in depth understanding of variety of methods in place for components used in Vaxcyte vaccine programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Result oriented; good judgment in directing attention and effort across competing priorities, especially when resource constrained; implements “best practices” or leading-edge quality standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly skilled in both verbal and written communication with the ability to interact effectively with people of diverse backgrounds and perspectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to integrate and interpret interdisciplinary project information; with at least a high-level understanding of the drug/vaccine development process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work globally with CMOs in different countries and continents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-starter and resourceful problem solver, able to move up learning curve with some guidance and map out intermediate milestones to achieve personal goals.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Director, Global Analytical Sciences and Technology (ASAT) Lead\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;Open to Remote; San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$166,000 – $194,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043044008,"name":"Analytical","child_ids":[],"parent_id":4043043008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5151345008?gh_jid=5151345008","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":4442328008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5151345008,"updated_at":"2026-03-18T13:02:10-04:00","requisition_id":"JR100067","title":"Senior Manager, Quality Control Data Analyst","company_name":"Vaxcyte","first_published":"2026-03-18T12:57:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte has an exciting opportunity for a Senior Manager, Quality Control Data Analyst to join our QC organization to act as a bridge between our technical QC Operations team and Business teams.\u0026amp;nbsp; This individual will be responsible for the collection, evaluation, interpretation, and visualization of complex datasets to provide actionable insights that drive technical and business decisions. Key responsibilities include creating reports, maintaining databases, and using tools to identify trends, initiate quality events if needed, improve efficiency, and support definition of acceptance criteria as well as strategic planning.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work closely with the analytical sub teams and other functions within Analytics, Process Development, Quality Assurance, Operations, and Regulatory functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accountable for data integrity, accuracy, and reliability as well as that datasets are assessed in a timely manner and meet quality and regulatory standards to ensure secure and uninterrupted supply of Vaxcyte’s innovative therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, implement, and maintain leading-edge analytics systems, taking complicated problems and building simple frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate internal systems for efficiency, problems, and inaccuracies with regard to data collection and evaluation, and develop and maintain processes and SOPs for handling, evaluation, and visualization of complex data sets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead activities in QC Operations with regards the data warehousing and data mining programs underway (VaxData).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain rich interactive visualizations through data interpretation and analysis, with reporting components from multiple data sources.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and implement data acquisition and integration logic, selecting an appropriate combination of methods and tools within the defined technology stack to ensure optimal scalability and performance of the solution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain databases by acquiring data from primary and secondary sources, and build scripts that will make our data evaluation process more flexible or scalable across datasets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement, and maintain robust quality control systems that encompass data mining, analysis, and visualization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow prescribed systems for data management, including secure storage, retrieval, and retention of QC data and documentation are in place. Ensure that all testing activities are well-documented and comply with Good Documentation Practices (GDP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In partnership with the analytical subteams and analytical science and technology, oversee data collection, evaluation and visualization for in-process and release data in order to support monitoring the analytical control strategy and related acceptance criteria.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify trends to initiate quality events and respective investigations through analysis of complex datasets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approval of analytical data, test reports, and certificates of analysis (CoAs) generated by contract laboratories to verify accuracy, completeness, and compliance with specifications for both in-process and release testing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact with IT for QC operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support investigations and deviations, out-of-specification (OOS), out-of-trend (OOT), out-of-expectation (OOE) results, laboratory incidents, and customer complaints collaborating with internal stakeholders to implement corrective and preventive actions (CAPAs) as a data Subject Matter Expert.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Writing, review and approval of documents related to Quality Control, Computer System Validation, and GAMP5 to ensure compliance with applicable regulatory and industry standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work directly with managers and users to gather requirements, provide status updates, and build relationships.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Bachelor’s degree (or equivalent) in biology, biochemistry or other related science with 8+ years of experience in biotechnology/pharmaceutical industry and 3+ years of experience as data analyst in data science/statistics. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven analytics skills, including mining, evaluation, and visualization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Technical writing experience in relevant areas, including queries, reports, and presentations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert level knowledge of the standard MS suite of programs (Excel, Word, VBA, Teams, Access).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong SQL, with aptitude for learning other analytics tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with database and model design and segmentation techniques.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Practical experience in statistical analysis through the use of statistical packages SPSS, and SAS.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive knowledge in cGDP and experience in multi-national regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving abilities, with a focus on data-driven decision-making and continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in Quality Control, especially late stage or commercial.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in a collaborative, team-oriented environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relentless focus and passion around process improvements (efficiency and automation).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Director, QC Business Operations\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt; $166,000 – $194,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043044008,"name":"Analytical","child_ids":[],"parent_id":4043043008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5188916008?gh_jid=5188916008","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":4459680008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5188916008,"updated_at":"2026-05-18T13:21:47-04:00","requisition_id":"643-340-2026","title":"Senior Manager, Supply Chain Planner","company_name":"Vaxcyte","first_published":"2026-04-16T12:08:37-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is seeking a strategic and execution-focused Senior Manager, Supply Chain Planner to join our Supply Chain \u0026amp;nbsp;Planning Team. This role is responsible for leading end-to-end supply planning across clinical and commercial programs, including demand and supply planning, capacity management, inventory strategy, and scenario analysis. The ideal candidate brings deep experience in biotech supply chains, strong systems and analytical capabilities, and a proven ability to translate complex data into actionable plans. This individual will play a critical role in driving cross-functional alignment, scaling planning processes and systems, and ensuring reliable supply to support Vaxcyte’s growth and commercialization objectives.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead end-to-end supply planning processes, including demand, supply, capacity, and inventory planning, ensuring alignment with business objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop integrated production and material plans using OMP Unison Planning System in collaboration with internal functions, CMOs, and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate monthly demand and supply reviews within the S\u0026amp;amp;OP process to align cross-functional stakeholders and enable informed decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuously improve planning processes, OMP Unison Planning system capabilities, and SOPs to enhance planning accuracy, efficiency, and scalability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain complex planning models, ensuring comprehensive system parameters and master data to support OMP and ERP integration\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and execute inventory strategies across raw materials, intermediates, and finished goods to balance service, cost, and expiry risk\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead scenario planning and “what-if” analyses to proactively identify risks and opportunities and implement mitigation strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor supply performance across CMOs to enable high-quality product delivery per plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, track, and communicate KPIs to provide actionable insights and support data-driven decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cultivate strong cross-functional and external partnerships to enable effective planning, communication, and execution\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S./B.A. required; advanced degree (MBA, MS, or equivalent) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of progressive supply chain planning experience in biotechnology, pharmaceuticals, or a related regulated industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in end-to-end supply planning, including demand, supply, capacity planning, and inventory optimization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with advanced planning systems (APS), preferably OMP Unison Planning, including implementation and process design\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive exceptional accuracy, precision, and data integrity across all planning activities, with a clear understanding of the substantial financial impact of supply decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience leading S\u0026amp;amp;OP processes and driving cross-functional alignment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and data modeling skills; advanced Excel required, experience with planning or visualization tools preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with external manufacturing networks in a GMP environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead scenario planning and risk mitigation to ensure continuity of supply\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership and influencing skills, with the ability to align diverse stakeholders and drive execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and executive presentation skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, with the ability to manage multiple priorities in a fast-paced, evolving environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented with a continuous improvement mindset and focus on operational excellence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Senior Director, Supply Planning\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Hybrid (minimum of 2-3 days per week)\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$176,000 - $205,000\u0026amp;nbsp;(SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is not eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4046547008,"name":"Global Supply Chain","child_ids":[],"parent_id":4043054008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5195819008?gh_jid=5195819008","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":4463059008,"location":{"name":"US - Remote"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Remote","value_type":"single_select"}],"id":5195819008,"updated_at":"2026-05-04T15:06:03-04:00","requisition_id":"694-770-2026","title":"Senior Medical Science Liaison","company_name":"Vaxcyte","first_published":"2026-04-27T19:56:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a scientifically driven and communicative Senior Medical Science Liaison (Sr. MSL) to join our Medical Affairs team. This field-based role is critical in supporting the scientific exchange around our vaccine pipeline, engaging with healthcare professionals (HCPs), public health experts, and key opinion leaders (KOLs). The Sr. MSL will play a pivotal role in advancing vaccine education, supporting immunization strategies, and informing internal teams with real-world insights.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced Stakeholder Management: Build and maintain peer-to-peer relationships with prominent physicians, researchers, key organizations, and high profile key opinion leaders (KOLs) at academic institutions and clinics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Scientific Engagement: Conduct peer-to-peer discussions with prominent physicians, researchers, and other key opinion leaders (KOLs) regarding unmet medical need, vaccine efficacy, safety, and public health impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical Education: Present clinical data and disease prevention strategies at conferences, advisory boards, and educational forums.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Public Health Collaboration: Partner with local and national public health organizations to support immunization campaigns and address vaccine hesitancy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advisory boards and conferences: Participate in and help organize advisory board meetings with KOLs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Vaxcyte at relevant medical conferences and scientific meetings, engaging in scientific exchange and gathering competitive intelligence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical Trial Support: Support in identification of clinical trial sites and provide scientific input on vaccine-related protocols and investigator-initiated studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Insight Collection: Gather field intelligence on emerging infectious disease trends, vaccination barriers, and unmet medical needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cross-functional collaboration: Work closely with internal teams to update/align scientific messaging and contribute to strategic planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Compliance: Uphold ethical standards and regulatory guidelines in all field activities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;Advanced degree (PharmD, PhD, MD, or equivalent) in life sciences, immunology, infectious diseases, or public health\u0026amp;nbsp;preferred\u0026lt;/span\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;At least 8 years relevant experience in a clinical, research, or industry-related medical role; experience in Medical Affairs preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Deep understanding of immunization science, epidemiology, and vaccine development.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Exceptional communication, presentation, and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;MSL positions are field-based and require significant travel, which can vary depending on the assigned territory. \u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-leveltext=\u0026quot;\u0026quot; data-font=\u0026quot;Symbol\u0026quot; data-listid=\u0026quot;1\u0026quot; data-list-defn-props=\u0026quot;{\u0026amp;quot;335552541\u0026amp;quot;:1,\u0026amp;quot;335559685\u0026amp;quot;:720,\u0026amp;quot;335559991\u0026amp;quot;:360,\u0026amp;quot;469769226\u0026amp;quot;:\u0026amp;quot;Symbol\u0026amp;quot;,\u0026amp;quot;469769242\u0026amp;quot;:[8226],\u0026amp;quot;469777803\u0026amp;quot;:\u0026amp;quot;left\u0026amp;quot;,\u0026amp;quot;469777804\u0026amp;quot;:\u0026amp;quot;\u0026amp;quot;,\u0026amp;quot;469777815\u0026amp;quot;:\u0026amp;quot;hybridMultilevel\u0026amp;quot;}\u0026quot; data-aria-posinset=\u0026quot;1\u0026quot; data-aria-level=\u0026quot;1\u0026quot;\u0026gt;Other combinations of education and/or experience may be considered.\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:160,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Senior Director, Medical Affairs\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Remote - United States\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$204,000 - $238,000\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4074310008,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4060325008,"name":"US - Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5205096008?gh_jid=5205096008","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":4467259008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Full-time","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5205096008,"updated_at":"2026-05-11T13:20:34-04:00","requisition_id":"723-920-2026","title":"Senior Veeva Systems Analyst","company_name":"Vaxcyte","first_published":"2026-05-05T12:03:19-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Veeva Configuration Specialist IT role serves as a techno-functional expert for Vaxcyte’s current and future Veeva applications and related technologies. Working closely with business and managed services partners, this role is responsible for implementing, managing, and maintaining Quality, Regulatory and Clinical Veeva Vault system configurations and other GxP and Non GxP enterprise applications. While technical in nature, this role drives business value by blending technology expertise with business process know-how. This is a hands-on role that reports to the Associate Director of Enterprise IT Systems at Vaxcyte’s San Carlos, California headquarters.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead requirements gathering, impact assessments, analysis, design, and configuration activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Customize and configure Veeva Vault applications to meet business requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Veeva admin and operational support for issues impacting end-users, system unavailability, data integrity, and manage user account provisioning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help develop and document business process flows.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain system-specific IT documentation such as configuration forms, business processes, operating procedures, templates and design standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain close working relationships with cross functional business partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with stakeholders to understand current business processes and identify areas for improvement and optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with other IT teams to ensure seamless integration with other systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide project management support for enhancement efforts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow GxP change management processes for system configuration changes and platform upgrades.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support periodic reviews and related compliance activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with managed services, business partners and assurance teams to implement planned releases and functional change requests.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in computer science, information systems, or related field.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;Minimum 3 years of hands-on configuration experience with any Veeva Vault Platform systems and minimum 7 years of total IT Systems experience. Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of Veeva application suites including Quality (QualityDocs, QMS, Vault Training), RIM and Clinical eTMF.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with validated GxP environments including implementation, documentation and change management is a must.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience as a business systems analyst for Enterprise IT systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Veeva system administration certification is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;As is/to be process mapping and analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid problem-solving skills and ability to troubleshoot issues including root cause analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills, with the ability to effectively communicate complex technical concepts to non-technical stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Technical writing skills for updating SOPs, WIs, Knowledgebase articles and documenting business processes.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Associate Director, IT Enterprise Systems\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;San Carlos, CA; Ability to be onsite 2 to 3 days a week.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$164,000 – $191,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043035008,"name":"IT","child_ids":[],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/4892976008?gh_jid=4892976008","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":4327542008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":4892976008,"updated_at":"2026-05-01T19:54:20-04:00","requisition_id":"JR100028","title":"Stability Manager ","company_name":"Vaxcyte","first_published":"2025-09-02T19:03:54-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vaxcyte is looking for an energetic and talented individual to join Vaxcyte’s Vaccine Product Development organization as a Stability Manager within the Quality Control Unit. The primary function of this level position is to manage the stability program for various projects in preclinical and clinical development.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The position will be an integral part of the team implementing and maintaining cGMP Stability for all phases of clinical development. Primary responsibility will include managing stability studies for individual projects and stability data analysis. This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations and documentation, foster open communication, and pursue data-driven approaches.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Functions:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Designs, coordinate, and execute stability studies for early and late-stage vaccine products according to regulatory guidelines and company protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Summarize vaccine stability results by applying analytical testing expertise to ensure scientific and technical excellence. Utilize statistical software like JMP to perform rigorous statistical analyses, ensuring robust interpretation of data and adherence to regulatory standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This includes, but not limited to, creating, implementing, and managing stability databases, performing data trending and statistical analysis, study and testing forecasting and reporting of metrics, creation, revision and approval of SOP\u0026#39;s, stability protocols and reports in accordance with current GMP, FDA, EU, Global and ICH guidelines and regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Produce impactful PowerPoint presentations to effectively communicate stability data to diverse project team members. Support the attainment of project milestones by facilitating stability monitoring and determining expiration dates for clinical and in-process materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Authors, reviews, revises, and approves SOP\u0026#39;s, stability protocols and reports, memo’s, regulatory and specification documents (as required).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The Stability Manager will also assist with leading the functionality and maintenance of stability related processes and systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives continuous improvement activities for the clinical stability programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures that the GMP stability program continuously aligns with FDA, ICH and other international agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages Quality Systems records for QC Stability- creates, assesses, reviews Deviations, Change Controls, CAPA\u0026#39;s and other applicable stability-related investigations and events.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Guide and work with others to identify opportunities for continuous improvement and implement/maintain solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strong teamwork in establishing a quality culture and shared accountability. Ensure GMP compliance is built into the design and implementation of processes and systems, including tracking metrics to monitor and improve performance.\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;MS or BS with minimum of 8 years of industry experience in Pharma / Biotech industry required.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;Other combinations of education and/or experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of vaccine stability principles, including degradation pathways, accelerated stability testing, and shelf-life determination.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated proficiency and expertise in various analytical methodologies, particularly in the context of stability testing and assessment of biologics or vaccines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of relevant FDA, EU, and ICH regulatory guidelines and pharmacopeia as applicable to stability study design, expiry dating, and analytical method qualification/validation for biologics and vaccines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding and hands-on experience of applying basic statistical tools for stability data trending and rate analysis to support retest period/ shelf-life proposals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and excellent skills in record keeping / documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in IND, NDA and BLA submission is highly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in a regulated (GLP / GMP) environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive technical writing experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills; ability to communicate effectively both verbally and in written formats.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of product development activities in biotech/drug/vaccine development, including key interdependencies, and knowledge of proven development strategies and tactics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work globally with CMOs in different countries and continents.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt; Director, Stability\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; San Carlos, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Compensation: \u0026lt;/strong\u0026gt;\u0026amp;nbsp;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt; $147,000 – $171,000 *(SF Bay Area). Salary ranges for non-California locations may vary.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043044008,"name":"Analytical","child_ids":[],"parent_id":4043043008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5193056008?gh_jid=5193056008","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":4461614008,"location":{"name":"Visp, Valais, Switzerland"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Onsite","value_type":"single_select"}],"id":5193056008,"updated_at":"2026-04-17T19:41:41-04:00","requisition_id":"743-315-B","title":"Vice President, Manufacturing Operations \u0026 Managing Director ","company_name":"Vaxcyte","first_published":"2026-04-17T19:41:41-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced and dynamic leader to join Vaxcyte as Vice President, Manufacturing Operations \u0026amp;amp; Managing Director for Vaxcyte Switzerland GmbH. This role will lead a high-performing operations organization in Switzerland, supporting late-stage development, commercial readiness, and long-term growth.\u0026amp;nbsp;The role will oversee critical capital projects, scale clinical and commercial supply capabilities, and provide strategic and operational leadership across a network of Contract Manufacturing Organizations (CMOs) in Europe to ensure reliable, compliant product supply.\u0026amp;nbsp;This position is accountable for both strategic and operational leadership of GMP activities. Strategically, the role will evolve the manufacturing network, strengthen key external partnerships, and ensure alignment with corporate objectives. Operationally, it will drive site performance, scale capabilities, and deliver program milestones. The role oversees Engineering \u0026amp;amp; Facilities, Manufacturing, Sourcing, and Supply Chain, with dotted-line leadership for MSAT and Quality Control in Visp.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Partnering closely with Process Development, Quality Assurance, and Regulatory, this role will drive facility performance and network execution while developing a deep understanding of program drivers and translating these into actionable plans across internal teams and CMOs.\u0026amp;nbsp;This role is critical to ensure timely, compliant, and uninterrupted supply of Vaxcyte’s therapies. Strong GxP knowledge and deep expertise in biologics manufacturing, engineering, and organizational leadership are required.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Essential Functions:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership, strategic direction, and risk-based oversight to translate corporate strategy into global manufacturing execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Take strong ownership of site success. Lead and manage the Vaxcyte Switzerland organization, including direct and matrixed reporting structures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and develop high-performing teams across Engineering \u0026amp;amp; Facilities, Manufacturing, Sourcing, Supply Chain, MSAT, and Quality Control.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and strategically manage CMO relationships, including participation in Joint Steering Committees (JSCs), ensuring alignment on quality, timelines, and cost.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee all CMO activities and commercial supply operations to ensure reliable, compliant delivery aligned with market needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead capital projects, including design, construction, startup, validation, and licensing of manufacturing facilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive facility performance, site master planning, continuous improvement, COGs reduction initiatives to support scalability and long-term growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and enhance manufacturing engineering and facilities capabilities supporting clinical and commercial supply.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and monitor KPIs and dashboards to track performance, risks, and progress across operations. Provide comprehensive performance reporting on the supply network to all relevant stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate closely with Process Development, Quality Assurance, Regulatory, and other cross-functional teams to ensure alignment and execution excellence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate resource planning internally and across CMOs, proactively addressing gaps, constraints, and risks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as escalation point for critical production or supply issues, leading cross-functional response.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop deep understanding of program priorities and translate into execution plans across internal teams and CMOs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Vaxcyte in external engagements, including governmental and regional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion operational excellence, continuous improvement, and strong GxP complian\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;MS in Science or Engineering with 20+ years of experience, or PhD with 15+ years of experience. \u0026amp;nbsp;15+ years of leadership experience in GMP manufacturing, operations, engineering, or large-scale biologics environments. Other combinations of education and/or experience may be considered.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven experience leading global manufacturing networks, including CMO oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success in facility startup, scale-up, and commercialization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience in microbial GMP manufacturing; multi-valent complex vaccines experience highly desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to build and lead high-performing, cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience establishing strong quality, safety, and continuous improvement cultures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong financial acumen, including capital project and budget management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience identifying and executing strategic investments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate at both strategic and operational levels with strong decision-making skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent leadership, communication, collaboration, and stakeholder management capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h4\u0026gt;Reports to: Chief Technical Operations Officer\u0026lt;/h4\u0026gt;\n\u0026lt;h4\u0026gt;Location: Visp, Switzerland\u0026lt;/h4\u0026gt;\n\u0026lt;h4\u0026gt;Compensation:\u0026amp;nbsp;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/h4\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4046549008,"name":"Swiss Manufacturing \u0026 Supply Chain","child_ids":[],"parent_id":4043054008}],"offices":[{"id":4036302008,"name":"Visp, Switzerland","location":"Visp, Valais, Switzerland","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5114728008?gh_jid=5114728008","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":4425394008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5114728008,"updated_at":"2026-06-02T00:30:43-04:00","requisition_id":"711-870-2026","title":"Vice President, Marketing","company_name":"Vaxcyte","first_published":"2026-02-13T14:44:16-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a Vice President of Marketing to lead our marketing strategy as we prepare to become a U.S. commercial vaccine company within the next 18 months. This role is critical to shaping our U.S. launch, building the marketing foundation for a first commercial product, and positioning the company for future global expansion.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate brings deep vaccine marketing experience, a strong understanding of the U.S. immunization landscape, and a proven track record of leading pre-launch and launch activities in a highly regulated environment. This leader will balance strategic vision with hands-on execution, building capabilities, teams, and processes appropriate for a first commercial launch. This individual should have demonstrated experience driving commercial demand across target audiences—including healthcare providers, consumers/patients, payers, and public health stakeholders—with a particular emphasis on consumer engagement strategies that build disease awareness and motivate vaccination behavior.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;U.S. Launch \u0026amp;amp; Commercial Strategy\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the development and execution of the U.S. marketing strategy for our initial vaccine launch, including disease awareness, brand positioning, and go-to-market planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop differentiated value propositions grounded in clinical data, public health impact, and real-world evidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Chief Commercial Officer to align marketing strategy with overall commercial, sales, and market access plans.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Vaccine \u0026amp;amp; Immunization Expertise\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Apply deep understanding of the U.S. vaccine ecosystem, including immunization schedules, CDC/ACIP considerations, public health stakeholders, and provider types.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design marketing strategies that address the unique dynamics of vaccine adoption, including site-of-care complexity, and public trust.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Medical Affairs and Regulatory to ensure compliant, scientifically sound communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Government Affairs and Policy teams to ensure marketing strategies account for evolving immunization policy, public funding mechanisms, and advocacy stakeholder dynamics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with HEOR and Market Access to develop evidence-based value narratives and payer-facing materials that support formulary positioning and access.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Brand \u0026amp;amp; Portfolio Marketing\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish the company’s commercial brand and narrative as we transition from a development-stage biotech to a commercial organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead brand development, messaging, and omnichannel promotional strategy across HCP, payer, and patient audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and execute integrated omnichannel engagement strategies spanning personal promotion, digital channels, and non-personal promotion to optimize customer reach, frequency, and impact across the vaccine adoption journey.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop digital-first engagement models for hard-to-reach HCP segments, including pharmacists and public health practitioners critical in vaccine delivery.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute consumer/patient engagement strategies—including disease awareness campaigns, direct-to-consumer (DTC) advertising, and health literacy initiatives—that drive vaccination demand at the population level.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build multi-audience demand generation strategies that create a pull-through effect across HCPs, consumers, payers, employers, and public health decision-makers to maximize vaccine adoption.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Patient Advocacy organizations and community health stakeholders to inform patient-centric messaging and overcome barriers to vaccination, including vaccine hesitancy and health equity gaps.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop lifecycle and indication expansion strategies to support future growth and pipeline advancement.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Market Insights \u0026amp;amp; Analytics\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead market research, customer insights, and competitive intelligence to inform launch readiness and ongoing optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define KPIs and performance metrics to measure marketing effectiveness and launch success.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage data analytics and AI-powered tools to enhance competitive intelligence, identify prescriber behavior patterns, and inform real-time marketing optimization decisions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Team, Infrastructure \u0026amp;amp; Capability Building\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and lead a high-performing marketing organization, scaling the team and capabilities over time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish agency partnerships and external vendors to support launch execution. Build and manage a high-performing agency roster with clear scopes of work, performance metrics, and governance structures that drive accountability and cost efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement marketing processes, governance, and operating models consistent with U.S. commercial and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement marketing operations infrastructure including project management systems, digital asset management (DAM), and content supply chain processes designed for scale and speed-to-market.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own the marketing budget, ensuring disciplined resource allocation across brand, digital, and promotional investments with clear ROI measurement and launch investment frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Future Global Expansion\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design U.S. marketing strategies with future global scalability in mind.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally to support early planning for potential international expansion, including global brand frameworks and knowledge transfer.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Digital Innovation \u0026amp;amp; AI-Enabled Marketing\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Champion the integration of AI and emerging technologies into marketing workflows to improve quality, speed, cost efficiency, and decision-making across the marketing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and deploy AI-powered tools for content creation, personalization, competitive intelligence, and customer engagement—ensuring all applications comply with regulatory and MLR requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage generative AI to accelerate content development cycles, enable omnichannel personalization at scale, and streamline the Medical-Legal-Regulatory (MLR) review process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish an AI-informed marketing operations model that uses predictive analytics to optimize targeting, message sequencing, and media mix allocation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities to use AI and automation to reduce agency costs, accelerate time-to-market for promotional materials, and improve ROI across marketing investments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with IT, Data Science, and Commercial Operations to build a connected, data-driven marketing ecosystem from the ground up.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree (MBA, MS, PhD) preferred with 15+ years of progressive marketing experience in biotech or pharmaceuticals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other combinations of education and/or experience may be considered\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Significant experience in vaccine marketing, including U.S. launch experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success leading pre-launch and first-launch marketing efforts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Preferred Qualifications:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience building a marketing organization in a pre-commercial or first-launch biotech environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track record of leading omnichannel marketing strategies integrating digital, non-personal, and field-based promotion.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing complex agency rosters and marketing vendor ecosystems across creative, media, digital, and analytics functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with AI/ML applications in marketing, including content generation, customer segmentation, predictive analytics, and campaign optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated fluency in marketing analytics, including KPI frameworks, attribution modeling, and data-driven optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with MLR processes and demonstrated ability to partner effectively with Medical and Legal/Regulatory in a compliant promotional environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong executive presence with the ability to influence C-suite stakeholders and represent the marketing function on cross-functional leadership teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience driving commercial demand generation across both HCP and consumer/patient audiences in a regulated healthcare environment, including DTC, disease education, or unbranded awareness campaigns.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Public health marketing or disease awareness campaign experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Chief Commercial Officer\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;East Coast - US\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$315,000 - $385,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is not eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-JN1\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043039008,"name":"Commercial","child_ids":[4070438008],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://boards.greenhouse.io/vaxcyte/jobs/5236929008?gh_jid=5236929008","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":4482739008,"location":{"name":"San Carlos, California, United States"},"metadata":[{"id":6839098008,"name":"Worker Sub-Type","value":"Regular","value_type":"single_select"},{"id":6871349008,"name":"Work Arrangement","value":"Hybrid","value_type":"single_select"}],"id":5236929008,"updated_at":"2026-06-04T11:44:00-04:00","requisition_id":"734-870-B","title":"Vice President, U.S. Market Access \u0026 Pricing","company_name":"Vaxcyte","first_published":"2026-06-04T11:44:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Join our Mission to Protect Humankind!\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;WHAT\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do is every bit as important as\u0026amp;nbsp;\u0026lt;strong\u0026gt;HOW\u0026lt;/strong\u0026gt;\u0026amp;nbsp;we do it!\u0026amp;nbsp;Our work together is guided by four enduring core values:\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;*MODEL EXCELLENCE:\u0026amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Summary:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Vice President, Market Access will lead the strategy and execution of all market access activities to support the successful launch of the company’s adult pneumococcal vaccine. Reporting to the Chief Commercial Officer, this role will be accountable for ensuring broad, timely, and sustainable access across public and private channels.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As Vaxcyte prepares for its first commercial launch, the VP will operate as a hands-on leader, building foundational capabilities while directly shaping payer, provider, and policy environments. This role requires a balance of strategic leadership and execution, with a particular focus on navigating the unique access dynamics of adult vaccines, including public health recommendations, buy-and-bill reimbursement, and site-of-care considerations.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Essential Functions:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead development and execution of the U.S. market access strategy for the adult pneumococcal vaccine, including pricing, reimbursement, contracting, and channel strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and drive launch readiness plans aligned to regulatory approval and immunization guideline milestones (e.g., ACIP or other recommending bodies)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Shape access strategies across commercial payers, Medicare, Medicaid, and public health channels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute engagement strategies for key stakeholders, including GPOs, IDNs, retail pharmacy, and public health entities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish pricing strategy and gross-to-net assumptions, ensuring alignment with vaccine-specific market dynamics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure readiness for coding, coverage, reimbursement, and provider economics within buy-and-bill and pharmacy settings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs to define and deliver HEOR and value evidence to support payer and policy decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the market access lead across cross-functional teams, aligning with Commercial, Medical, Regulatory, Government Affairs, and Finance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and lead a lean market access function, leveraging external partners to scale capabilities efficiently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working cross functionally, prepare for CDC immunization program, state immunization program, and ACIP-adjacent policy stakeholder engagements; translate ACIP recommendation language into access and coverage implications across all channels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute integrated PBM, commercial payer, and Medicare Part B and D contracting strategies to ensure optimal formulary positioning, coverage, and patient access across channels.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development of national retail pharmacy and alternate vaccination site strategies, establishing partnerships that maximize vaccine availability, administration, and uptake.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop scenario-based access, reimbursement, and customer adoption strategies aligned to potential ACIP recommendation outcomes and evolving adult immunization guidelines\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree (MBA, MPH, PharmD, PhD) preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;15+ years of experience in market access, pricing, reimbursement, or related functions within biotech/pharma\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience supporting or leading product launches, ideally in vaccines, infectious disease, or buy-and-bill products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of adult vaccine access dynamics, including public health recommendations, Medicare Part B and Part D reimbursement, Medicaid, 340B program implications, CDC contract vehicles (Section 317 and VFC), and site-of-care economics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience operating in lean or pre-commercial biotech environments, with a demonstrated track record of building market access capabilities from the ground up\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to balance strategic thinking with hands-on execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional leadership and stakeholder influence skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing gross-to-net financial modelling, including rebate strategy across payers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to work collaboratively with HEOR teams to translate cost-effectiveness models, budget impact analyses, and payer value dossiers into P\u0026amp;amp;T committee submissions or ICER reviews\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior engagement with CDC immunization programs, state immunization programs, or ACIP-adjacent policy processes; understanding of how ACIP recommendation language drives uptake across channels\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Reports to: \u0026lt;/strong\u0026gt;Chief Commercial Officer\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;East Coast - US\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Hybrid (minimum of 2-3 days per week) / Remote\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Compensation:\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Salary Range: \u0026lt;/strong\u0026gt;$333,000 - $388,000 (SF Bay Area). Salary ranges for non-California locations may vary.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Relocation:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;This role is eligible for relocation assistance.\u0026amp;nbsp;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4043039008,"name":"Commercial","child_ids":[4070438008],"parent_id":4043029008}],"offices":[{"id":4036301008,"name":"San Carlos, California","location":"San Carlos, California, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":55}}