{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4205085009","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":4119819009,"location":{"name":"Remote"},"metadata":null,"id":4205085009,"updated_at":"2026-05-27T09:07:47-04:00","requisition_id":"221","title":"Associate Director, GxP Systems","company_name":"Vera Therapeutics, Inc.","first_published":"2026-04-06T15:38:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, GxP Systems will report to the Sr. Director, Commercialization Systems and will be responsible for leading the implementation, validation, and support of GxP-regulated systems to enable Quality Assurance, Regulatory, Clinical, and Process Development \u0026amp;amp; Manufacturing (PD\u0026amp;amp;M) in a commercial biotech environment. This role will play a pivotal part in supporting regulatory, compliance, and for commercialization. Working with Quality Assurance, Medical Affairs, Regulatory Affairs, Clinical Operations, and PD\u0026amp;amp;M functions to ensure systems are fit-for-purpose, validated and aligned with evolving business requirements.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the System Owner and hands-on administrator for GxP systems (e.g., TraceLink, Lorenz DocuBridge, Egnyte Life Sciences, ZenQMS, Global Vision, Veeva), overseeing system lifecycle, performance, and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in system implementation activities, including vendor selection, requirements gathering, testing, and deployment to ensure alignment with business and regulatory needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight and direction for Computer System Validation (CSV) activities and validation documentation, partnering with the Validation Engineer to ensure regulatory compliance and audit readiness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and lead Change Control processes for all GxP systems, including impact assessments, risk evaluations, documentation, coordination of testing, and release management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform system administration activities, including user access provisioning, role management, periodic access reviews, and audit trail monitoring\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee system maintenance, enhancements, and issue resolution (e.g., upgrades, patches, changes), ensuring appropriate validation impact assessments, documentation updates, and minimal business disruption\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with IT and vendors to support integration, system performance optimization, and resolution of technical issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain system-related documentation, including SOPs, Systems Inventory, administrative procedures, and work instructions in collaboration with Quality Assurance and business stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide SME support during FDA audits and inspections, including preparation, documentation review, and representation of system controls and validation status\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous improvement by identifying gaps, inefficiencies, and opportunities for system scalability and automation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate business requirements into effective system solutions, acting as a key liaison between business stakeholders and technical teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage project timelines, risks, and deliverables to ensure successful and compliant execution of system initiatives\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences, Information Systems, Computer Science, Engineering, or a related field; advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10-12 years of hands-on experience with GxP systems in Life Sciences, including system administration, validation oversight, and operational support\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience implementing and validating systems such as eQMS, TraceLink, LMS, Validated Documents and Data storage solutions (such as Box for GxP or Egnyte Life Sciences), or ERP systems (e.g., NetSuite, Oracle, SAP) in a GxP-regulated environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of CSV, data integrity, Part 11 compliance, and regulatory expectations (FDA, EMA, ICH)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience partnering with validation/CSV resources while maintaining accountability for system compliance and validation outcomes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience owning and managing Change Control processes for GxP systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting pre-commercial biotech organizations transitioning to commercialization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance strategic oversight with hands-on system administration and operational responsibilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional collaboration skills across IT, QA, Regulatory, and Technical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing vendors and implementation partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent troubleshooting, analytical, and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills with the ability to translate technical concepts into business terms and influence stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$145,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$220,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006091009,"name":"Information Technology","child_ids":[],"parent_id":null}],"offices":[{"id":4006146009,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4203209009","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":4118630009,"location":{"name":"Brisbane, CA"},"metadata":null,"id":4203209009,"updated_at":"2026-04-29T14:12:42-04:00","requisition_id":"218","title":"Executive Assistant to the Office of the Chief Business Officer (CBO)","company_name":"Vera Therapeutics, Inc.","first_published":"2026-04-01T17:23:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Executive Assistant role will report to the Chief Business Officer (CBO) and will act as a partner to executives across the office of the CBO, including Corporate Communications, Portfolio \u0026amp;amp; Program Management, and Business Development \u0026amp;amp; Alliance Management functions. This role is ideal for someone who thrives in fast-moving environments, brings structure to ambiguity, and can seamlessly shift between executive support and operational coordination. This role enables leadership to stay focused on strategy and growth by ensuring administrative priorities and cross-functional initiatives continue moving forward despite ambiguity and shifting priorities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Executive \u0026amp;amp; Leadership Support\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage complex executive calendars, travel, expense reporting, and meeting prioritization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare briefing notes and key materials for internal and external meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate meetings and track action items.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help track department budgets.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Project \u0026amp;amp; Operational Coordination\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support portfolio/program management activities and cross-functional coordination.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track priorities, risks, and dependencies across initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Communications \u0026amp;amp; Corporate Initiatives\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support internal communication platforms and staff company-wide events.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee scheduling of corporate-wide events and event management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage contracts and SOWS with external consultants and speakers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with other EAs on internal events.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Business Development Support\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Coordinate materials and logistics for business development meetings and partner interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with coordination of external conferences, partner meetings, and other business development engagements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support diligence processes by organizing materials, timelines, and internal coordination.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in tracking BD opportunities and maintaining internal trackers.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS degree with 2-3+ years of experience supporting senior executives or leading operational coordination in biotech, consulting, or high-growth environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting business development, strategy, or corporate functions preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and comfort managing multiple priorities that change quickly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear, concise communicator who can work effectively across functions and levels.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive, resourceful, and comfortable operating with limited direction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates a high level of discretion, ownership, and accountability when handling sensitive information and supporting executive-level priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly proficient with productivity and collaboration tools including Microsoft Office (Excel, PowerPoint), Slack, Box, and modern AI productivity tools (e.g., ChatGPT, Claude).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$95,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$131,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006093009,"name":"G\u0026A","child_ids":[],"parent_id":null}],"offices":[{"id":4006145009,"name":"Brisbane (Hybrid)","location":"Brisbane, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4260511009","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":4152431009,"location":{"name":"Brisbane, CA "},"metadata":null,"id":4260511009,"updated_at":"2026-06-09T12:43:44-04:00","requisition_id":"237","title":"Payroll Manager","company_name":"Vera Therapeutics, Inc.","first_published":"2026-05-28T14:23:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Payroll Manager reports to the Associate Director, Accounting Operations, and is responsible for accurate and timely payroll processing, accounting and other accounting functions related to employee benefit plans. This role also supports related monthly close activities, SOX compliance, and financial statement audits.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage the semi-monthly, multi-state payroll processing ensuring accuracy, compliance, and adherence to internal deadlines including W‑2s, tax filings, and benefits (health insurance, 401(k), FSA, stock compensation).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage ad hoc payroll processing as needed for stock compensation transactions and mid-period employee exits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with federal, state, and local tax and labor regulations, as well as internal controls expectations such as SOX compliance, while staying current with evolving legislation and industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and execute payroll audits, including ongoing reconciliations of payroll accounts, tax withholdings, benefits contributions, and other deductions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and analyze payroll reports, conduct audits to identify discrepancies or issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work cross-functionally to support compliance and operation of employee benefit plans, such as 401(k), and take a lead role in managing required plan audits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the primary escalation point for complex payroll issues, investigating and resolving discrepancies, and addressing concerns from employees and other departments such as HR and external providers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Accounting and HR to ensure payroll operations are well-documented, audit-ready, and aligned with evolving compliance expectations as the company scales.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion continuous process improvement; identify opportunities to automate workflows, reduce errors, and scale payroll operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with the application and registration for new tax IDs as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and monitor earnings and deductions codes used for payroll processing and the related GL account mapping on the ADP GL Report.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in accounting or related field preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years’ experience in payroll and equity accounting, with biotech or life science industry and public-company experience preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with ADP Workforce Now payroll system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Equity Edge Online.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with ERP systems, preferably NetSuite.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of payroll tax laws, and labor regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multitask and work under pressure to meet strict deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and in a team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and problem-solving skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with auditors and SOX compliance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$125,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$155,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006099009,"name":"Accounting \u0026 Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4006145009,"name":"Brisbane (Hybrid)","location":"Brisbane, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4140120009","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":4092050009,"location":{"name":"Remote"},"metadata":null,"id":4140120009,"updated_at":"2026-04-29T14:12:42-04:00","requisition_id":"204","title":"Senior Director, Risk Management, DSPV","company_name":"Vera Therapeutics, Inc.","first_published":"2026-03-04T16:58:44-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Risk Management, Drug Safety \u0026amp;amp; Pharmacovigilance (DSPV) will report to the Vice President, Drug Safety \u0026amp;amp; Pharmacovigilance and will be responsible for our Risk Management strategy and Benefit Risk Office at Vera which strives for excellence and the creation of a best practice framework. As a Risk Management Lead, you will be empowered to work cross-functionally with colleagues to establish and manage the processes for Risk Management, benefit risk, RMPs, additional Risk Minimization Measures and REMS programs and other Benefit Risk deliverables. The overall goal of the Risk Management Lead is to optimize the proactive impact made by the PV department at Vera while maximizing patient safety and minimizing/preventing patient risk.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serves as Project manager of the PV Risk Management System to oversee, evaluate, characterize, strategize, implement, assess and track vera’s PV Risk Management obligations, commitments and proposed minimization measures to ensure patient safety is at the forefront of DSPV.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide recommendations and guidance through subject matter expertise on risk management and risk minimization strategy to an assigned therapeutic area to ensure that product risk management strategies are consistent worldwide.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide recommendations and guidance through subject matter expertise on the structured benefit risk assessment framework and the development of the benefit risk assessment documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with cross-functional teams (e.g. Clinical Development, Clinical Operations, Medical Affairs, Regulatory Affairs, and Biostats) to ensure alignment of Vera’s global position for the PV risk management processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic expertise to cross-functional product team members in developing pharmacovigilance risk strategies including benchmarking and scenario planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the development of risk management plans (RMPs) in modular format, review RMPs) and ensure alignment with Good Pharmacovigilance Practices and other applicable regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Remain up to date and well informed on all Regulatory intelligence as it relates to risk management and relay this to the Project team and the PV medical safety science team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Aide in the development and review risk minimization documents such as Developmental RMPs, RMPs, risk minimization measures and Risk Evaluation and Mitigation Strategy (REMS).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide subject matter expertise and thoughtful contributions to qualitative and quantitative structured benefit risk assessments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance on incorporation of the patient’s perspective into benefit-risk activities (e.g. Real-World Evidence studies with Medical Affairs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with PV Physician Leads, Clinical Leads, PV scientists and Clinical Research Scientists, and others cross-functional teams on benefit risk assessment strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and provide recommendations for appropriate risk management interventions such as direct healthcare professional communications, educational materials, controlled access program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance and drive the creation of tracking risk management commitments including utilization of a tracking spread sheet or platform and improvement assessments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and report risk management metrics to ensure compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide centralized support, training, and leadership for safety and cross-functional members who work on risk management plans and risk minimization activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support inspections and audit activities internally and externally with regards to risk management processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties as defined in standard operation procedures or requested by supervisor.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with PV Physician and PV Scientists to aide in the proper characterization and classification of Risk from initial signal to evaluation, validation, implementation in study documents, protocols, IBs, ICFs, and RMPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with VP of DSPV, PV Physicians and PV Scientists on any Regulatory Submission/filing for BLA, SBLA, MAA, etc. to be sure that risks are reflected properly and carried through to support filing activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee risk components of Aggregate reports like DSUR, PBRER etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with PV Physicians and PV Scientist in risk presentations at safety Governance meetings (MSRB \u0026amp;amp; MSRC) to ensure proper communication of risk is achieved and proper course of action is followed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and oversee any outsourced RMP related activities to external vendors.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD/Pharmacist/ PharmD/DO/MD with 12+ years of experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5-10 years in PV/safety OR clinical development preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 5-10 years of pharmaceutical industry/drug development experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pharmaceutical industry experience, with exposure to PV risk management, additional risk minimization measures, and/or REMS programs preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong track record of scientific and analytical thinking.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience presenting at meetings is desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with integrity and work proactively in a fast-moving environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good Critical thinking skills. Ability to use good analytical/judgment skills to understand, analyze, and communicate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project Management Skills with ability to manage both time and priority constraints and to manage multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail, computer literacy, knowledge of safety databases.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Good working knowledge of all the functions within PV from PV operations onto medical safety science and all processes in between.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$220,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$305,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006100009,"name":"Pharmacovigilance","child_ids":[],"parent_id":null}],"offices":[{"id":4006146009,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4206091009","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":4120409009,"location":{"name":"Brisbane, CA"},"metadata":null,"id":4206091009,"updated_at":"2026-04-29T14:12:42-04:00","requisition_id":"222","title":"Senior Manager, Quality Assurance","company_name":"Vera Therapeutics, Inc.","first_published":"2026-04-06T15:34:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Manager, Quality Assurance (QA), will report to the Director, QA Drug Substance and is primarily responsible for QA function for Cell Bank and Drug Substance (DS). The position is responsible for collaborating with cross-functional teams and external partners to ensure both clinical and commercial Drug Substances meet regulatory requirements and internal Vera standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the oversight of the quality and compliance, primarily cell bank and biologics DS manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support implementation of strategies and tactics to promote and maintain GxP compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide quality support on tech transfers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Liaise with CMO Quality partners to communicate QA policy and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with contract manufacturers and internal stakeholders to address deviations/ investigations and compliance issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for material disposition of cell banks, commercial and clinical DS.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review executed batch records and associated documentation for material disposition.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve GMP documentation such as master batch records, deviations, change controls, specifications, and various other protocol and reports to support GMP production.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide quality support for validations including process validation, shipping validation, cleaning validation, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides support during both internal and regulatory agency audits as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform Person-in-Plant duties, as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in Material Review Board as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Helps define and implement appropriate quality standards/specification, methods, systems, and metrics for clinical and commercial quality operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the Quality representative on assigned product teams to advocate compliance and quality assurance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in Quality Agreements negotiation with external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support product lifecycle and continued process verification.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Availability for 5-15% travel, both domestically and internationally.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree with 10+ years of experience in biomedical engineering, chemical engineering, pharmaceutical sciences, or a related field or a Master’s degree with 7+ years of experience in biomedical engineering, chemical engineering, pharmaceutical sciences, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 6+ years of experience in a GMP Quality, Compliance, and/or Regulatory setting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 6+ years in a GMP QA role, and preferably direct work experience in either Manufacturing or QC, as well.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, including demonstrated ability to effectively communicate in a project team environment, within department, among functional groups and among external collaborators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Innovative skills with problem solving and peer influence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth knowledge of FDA, ISO, EMA, GMP and ICH quality systems and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience of working with external partners and biologics DS manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with Cell Bank is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with process validation is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail is a must.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, written and oral communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate in a fast-paced, multi-disciplinary industrial environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable and comfortable with normally receiving no instructions on routine work and general instructions on new assignments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$140,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$190,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006098009,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4006145009,"name":"Brisbane (Hybrid)","location":"Brisbane, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4219356009","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":4128377009,"location":{"name":"Remote"},"metadata":null,"id":4219356009,"updated_at":"2026-04-29T14:12:42-04:00","requisition_id":"226","title":"Senior Manager, Quality Assurance","company_name":"Vera Therapeutics, Inc.","first_published":"2026-04-21T08:51:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Senior Manager, Quality Assurance\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Drug Product\u0026lt;/strong\u0026gt; focus, will report to the \u0026lt;strong\u0026gt;Director, Quality Assurance\u0026lt;/strong\u0026gt;. The Senior Manager is responsible for collaborating with cross-functional teams and external partners to ensure both clinical and commercial Drug Products and Devices meet regulatory requirements and internal Vera standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for quality oversight of biologics sterile drug product (DP) manufacturing and combination products, including design control and Design History File (DHF) requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for implementing strategies and tactics to promote and maintain GxP compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead quality aspects of and provide quality support on DP tech transfers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Liaise with CMO Quality partners to communicate QA policy and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with contract manufacturers and internal stakeholders to address deviations/ investigations and compliance issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for material disposition of commercial and clinical DP/ combination products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review executed batch records and associated documentation for material disposition.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve GMP documentation such as master batch records, deviations, change controls, specifications, and various other protocol and reports to support GMP production.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve validation protocols and reports such as process validation, shipping validation, cleaning validation, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides assistance during both internal and regulatory agency audits as required\u0026lt;br\u0026gt;Perform Person-in-Plant duties, as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in Material Review Board as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Helps define and implement appropriate quality standards/specification, methods, systems, and metrics for clinical and commercial quality operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the Quality representative on assigned product teams to advocate compliance and quality assurance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead for Quality Agreement with external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support product lifecycle and continued process verification.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Availability for 10-20% travel, both domestically and internationally.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biomedical engineering, chemical engineering, pharmaceutical sciences, or a related field. Advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 10+ years of experience in a GMP Quality, Compliance, and/or Regulatory setting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 6+ years in a GMP QA role, with a preference for direct experience in biologics sterile DP manufacturing/aseptic processing including vials and prefilled syringes/autoinjectors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, including a demonstrated ability to effectively communicate in a project team environment, within department, among functional groups and among external collaborators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Innovative skills with problem solving and peer influence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth knowledge of FDA, ISO, EMA, GMP and ICH quality systems and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience of working with external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail is a must.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, written and oral communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate in a fast-paced, multi-disciplinary industrial environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable and comfortable with normally receiving no instructions on routine work and general instructions on new assignments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiar with global medical device/combination products standards such as 21 CFR Parts 803, 806, and 820, ISO 13485, and EU MDR is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$127,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$193,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006098009,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4006146009,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4253915009","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":4148507009,"location":{"name":"Brisbane, CA "},"metadata":null,"id":4253915009,"updated_at":"2026-05-28T14:13:53-04:00","requisition_id":"232","title":"Senior Manager, Regulatory CMC","company_name":"Vera Therapeutics, Inc.","first_published":"2026-05-28T14:13:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera is seeking a Senior Manager, Regulatory CMC to join an experienced, fast-paced and collaborative team. The Senior Manager will report to the Senior Director of Regulatory CMC and will be responsible for\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;working with the cross-functional team\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;to lead and support regulatory submissions and activities in the US and globally to support development programs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proactively manage CMC aspects of clinical products in early-to-late development to create high quality regulatory submissions that support product development strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review CMC modules of applications and amendments for submission, ensuring complete regulatory content that meets current regional requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Regulatory Affairs on cross-functional project teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate proposed manufacturing changes for impact to existing filings and providing strategic regulatory guidance for optimal implementation of changes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and implement internal regulatory processes, author and review SOPs and Work Instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate, track, and prioritize regulatory activities and associated resources, ensuring they are functional, consistent, and integrated to reflect cross-functional dependencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Determine risk assessment and implement regulatory strategies for products in early-to-late development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure regulatory compliance with relevant regulations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge and experience in interpretation of global regulatory requirements, with particular emphasis on the US region.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and the ability to track multiple timelines in parallel and manage deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication and ability to collaborate across functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving skills and attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience communicating regulatory strategies to stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated regulatory affairs experience commensurate with the role; BA/BS in a scientific field and a minimum of 6 years of relevant experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Industry experience in CMC development of biologics preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with a regulatory information management system, such as Veeva Vault RIM a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$140,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$214,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006085009,"name":"Regulatory","child_ids":[],"parent_id":null}],"offices":[{"id":4006146009,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4273981009","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":4159880009,"location":{"name":"Remote"},"metadata":null,"id":4273981009,"updated_at":"2026-06-09T12:45:00-04:00","requisition_id":"239","title":"Vice President, Commercial Manufacturing Operations","company_name":"Vera Therapeutics, Inc.","first_published":"2026-06-05T17:24:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Vice President, Manufacturing Operations will report to the SVP Product Development and Manufacturing (PD\u0026amp;amp;T) and will be responsible for leading the transition from a clinical-stage organization to an effective commercial manufacturing organization. As a key partner to the SVP PD\u0026amp;amp;T, the candidate will lead and develop a best-in-class manufacturing and supply chain team that can collaboratively work across functions to enable commercial launch of our lead product into global markets.\u0026amp;nbsp; While working with internal teams, such as quality, regulatory, commercial, and finance, and external contract service provides, the individual is responsible for ensuring that the end-to-end supply chain is set up to meet the global commercial product demand with keen eye towards continuous process improvement.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leads the manufacturing and supply chain teams, providing leadership aligned with Vera values resulting in a high performing organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contributes to the strategic leadership of Vera’s late-stage programs acting as a strong team player\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in sales and operations planning (S\u0026amp;amp;OP) and Product Development Teams representing the Product Development and Manufacturing function\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create synergy and knowledge sharing to enable optimal production planning processes to balance supply/demand risks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serves as a single point of contact to manage end-to-end global supply chain and foster the needed supplier relationships to drive excellence using appropriate metrics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serves as a strategic thought leader to craft and manage commercial supply contracts with an eye towards life cycle extension programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create, develop and manage necessary tools for end-to-end demand/supply planning\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic direction, technical guidance, and long-range planning for late-stage programs: BLA-enabling studies through BLA submission, commercial launch, and sustaining operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage department budgets and ensure fiscal responsibility for manufacturing operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop fit for purpose operational processes and systems to support supplier metrics and other tools to enable continuous improvement / process excellence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences or Engineering required. Master\u0026#39;s degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;15+ years of relevant experience from biopharmaceutical manufacturing required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of senior-level line management experience leading other leaders required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of creating business results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep technical, operational, regulatory, strategic, and quality expertise, along with a proven track record of leading late-stage programs in innovative biotech or pharmaceutical organizations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with operating and navigating regulatory requirements including authoring and reviewing BLAs and interacting with regulatory authorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of drug development within the biopharmaceutical industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience within development and manufacturing of monoclonal antibodies or related field preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal skills, collaborative leadership style\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads by example in recognizing and modeling Vera values.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Learning agility: ability to seek input, make connections, recognize patterns that lead to effective decision-making and action.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to thoughtfully evaluate processes, identify opportunities for improvement and successfully execute on those plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills (oral \u0026amp;amp; written); able to effectively interact with all levels internally and externally – able to tailor communications to the audience to achieve desired results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail with ability to move easily between hands-on work and strategic thinking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multitask and prioritize.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership skills with a desire to nurture, train, and grow the existing finance group\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to influence and deliver results in a virtual (outsourced) environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$248,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$375,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006082009,"name":"CMC","child_ids":[],"parent_id":null}],"offices":[{"id":4006146009,"name":"Remote","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4174687009","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":4101131009,"location":{"name":"Remote"},"metadata":null,"id":4174687009,"updated_at":"2026-04-29T14:12:42-04:00","requisition_id":"210","title":"Vice President, Regulatory Affairs","company_name":"Vera Therapeutics, Inc.","first_published":"2026-03-31T10:17:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell–mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit \u0026lt;a href=\u0026quot;http://www.veratx.com/\u0026quot; data-auth=\u0026quot;NotApplicable\u0026quot; data-linkindex=\u0026quot;2\u0026quot;\u0026gt;www.veratx.com\u0026lt;/a\u0026gt;.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do—from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Vice President, Regulatory Affairs\u0026lt;/strong\u0026gt; will be responsible for the development and execution of the company’s Regulatory strategy and report into the \u0026lt;strong\u0026gt;Senior Vice President, Regulatory and Quality\u0026lt;/strong\u0026gt;.\u0026amp;nbsp; This critical hire will provide input, prioritize, implement, monitor, and communicate Vera’s Regulatory strategy and programs.\u0026amp;nbsp; As part of the Quality and Regulatory leadership team, you will establish and translate Vera’s Regulatory strategy into operational policies, processes, procedures, and training to meet global regulatory, medical/health, and legislative standards.\u0026amp;nbsp; This role requires experience, knowledge, and leadership credibility to be effective across Vera in multiple capacities, thereby ensuring compliance with Regulatory standards and corporate-wide commitment to Quality principles and Vera values.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Additional representative responsibilities will include, but not necessarily be limited to, the following:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In this highly visible role, the successful candidate will develop and lead integrated global regulatory strategies (US, EU, and key ex‑US markets) for all pipeline programs, aligning with overall corporate and clinical development goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a primary regulatory strategist providing clear assessments of regulatory options, risks, and timelines to inform portfolio and investment decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee planning, authoring, review, and submission of regulatory dossiers including pre‑IND/IMPD packages, INDs/CTAs, IBs, pediatric plans, orphan/expedited program requests, DSURs/PSURs, NDAs/BLAs/MAAs, and post‑approval supplements/variations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead or directly oversee global health authority interactions (e.g., FDA, EMA, PMDA and key national agencies), including scientific advice/protocol assistance, Type B/C meetings, pre-submission and advisory committee preparations; ensure high‑quality briefing packages and robust meeting follow‑up.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with cross-functional teams to ensure clinical trial designs, endpoints, and statistical plans are aligned with regulatory expectations and support future registration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee global CMC regulatory strategies, including module 3/quality sections, comparability plans, and lifecycle management; ensure alignment with GxP and ICH requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely, accurate maintenance of all active INDs/CTAs and marketing authorizations, including safety reports, annual reports, labeling updates, and other commitments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, lead, and mentor a high‑performing regulatory team effectively leveraging external consultants, CROs, and vendors for eCTD publishing and ex‑US submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and continuously improve phase‑appropriate regulatory processes, standards, and governance (e.g., submission planning, HA interaction tracking, labeling governance) suitable for a lean organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay current on evolving global regulatory requirements, guidance, and precedent, and proactively incorporate learnings into program strategies and company policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support business development activities by contributing regulatory due diligence, risk/benefit assessments, and integration planning for potential partnerships, in‑licensing, and acquisitions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Regulatory Affairs on cross‑functional governance bodies and, as needed, with partners, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in life sciences or related discipline (e.g., PhD, PharmD, MD, or MS); equivalent experience may be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;15+ years of increasing responsibility in biopharmaceutical regulatory affairs, including substantial experience in small or mid‑size biotech environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of leading major global submissions (IND/CTA and NDA/BLA/MAA or equivalent) through acceptance and, ideally, approval.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience interacting directly with FDA, EMA and other global health authorities, including leading meetings and negotiations on complex issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of global regulatory frameworks (ICH, FDA, EMA and other regional requirements) across early development, registration, and post‑approval lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience overseeing or partnering with CMC, regulatory operations/electronic submissions (eCTD), and safety/periodic reporting activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to build, lead, and develop teams, and to work effectively as both a hands‑on individual contributor and strategic leader in a lean, fast‑paced biotech setting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, with the ability to convey complex regulatory concepts clearly to both technical and non‑technical audiences, including senior leadership and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High degree of integrity, sound judgment, and a pragmatic, solutions‑oriented mindset with strong organizational and project management skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Vera Therapeutics Inc. is an equal-opportunity employer.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;For this role, the anticipated base pay range is\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$259,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$394,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;line-height: 1;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Notice to Recruiters/Staffing Agencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vera Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Vera Therapeutics and such organization and will be considered unsolicited and Vera Therapeutics will not be responsible for related fees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Fraud Alert\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;To all candidates: your personal information and online safety are a top priority for us. At Vera Therapeutics, recruiters only direct candidates to apply through our official career page at\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://veratx.com/careers/\u0026quot;\u0026gt;https://veratx.com/careers/\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Recruiters will always contact you using the domain of veratx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Vera Therapeutics, please email human resources.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4006085009,"name":"Regulatory","child_ids":[],"parent_id":null}],"offices":[{"id":4006145009,"name":"Brisbane (Hybrid)","location":"Brisbane, California, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":9}}