QA Manager
US$150,000 – US$189,000 / yr base salary
Posted 13 Aug 2026
Advertised as “Senior QA Manager, GMP GxP Auditing & Vendor Management”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 8+ yrs
- Management level
- People management
- Employment
- Remote
- Contract
- Full-time
| Base salary | US$150,000 – US$189,000 / yr |
|---|
CertificationsASQ Certified Quality Auditor
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
The Opportunity:
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Lead GxP internal audits and external audits including completing audit reports and follow-up on corrective actions.
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Maintain the internal/external audit schedules.
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Assure GMP/GxP compliance with suppliers.
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Oversight of all aspects of GxP vendor / supplier program management to ensure compliance with GxP regulations and RevMed internal standards.
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Demonstrate the ability to multi-tack. Prioritize work and independently solve problems.
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Collaborate with vendors and internal teams to draft and complete Quality Agreements.
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Perform Risk Assessments, qualifications, and monitor Suppliers/CMOs.
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Collaborate with cross-functional teams and represent Quality Vendor Management at meetings.
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Create and implement any tools to improve compliance, consistency, and efficiency for GMP/GXP auditing and Vendor management.
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Provide support preparation of anticipated regulatory inspections (including those at contracted organizations), and partner audits with cross-functional teams.
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Maintain supplier management program, ensuring requirements, plans, processes, metrics, and tracking system for GxP suppliers are established and followed.
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Responsible for qualifications of GMP suppliers including performing audits, generation of audit reports, and follow- up with suppliers for addressing observations from audits.
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Negotiate, draft, and manage quality technical agreements (QTA) and/or contracts with suppliers, ensuring alignment with internal standards, regulations, and industry standards.
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Lead meetings for alignment, communication, and resolution of issues.