New · posted Oct 23
Revolution Medicines · Biotechnology
Senior QA Manager, GMP GxP Auditing & Vendor Management
- Redwood City, CA
- On-site
- Full-time
- Manager
Open until filled
The role
Lead GxP internal audits and external audits including completing audit reports and follow-up on corrective actions.
Maintain the internal/external audit schedules.
Assure GMP/GxP compliance with suppliers.
Oversight of all aspects of GxP vendor / supplier program management to ensure compliance with GxP regulations and RevMed internal standards.
Demonstrate the ability to multi-tack. Prioritize work and independently solve problems.
Collaborate with vendors and internal teams to draft and complete Quality Agreements.
Perform Risk Assessments, qualifications, and monitor Suppliers/CMOs.
Collaborate with cross-functional teams and represent Quality Vendor Management at meetings.
Create and implement any tools to improve compliance, consistency, and efficiency for GMP/GXP auditing and Vendor management.
Provide support preparation of anticipated regulatory inspections (including those at contracted organizations), and partner audits with cross-functional teams.
Maintain supplier management program, ensuring requirements, plans, processes, metrics, and tracking system for GxP suppliers are established and followed.
Responsible for qualifications of GMP suppliers including performing audits, generation of audit reports, and follow- up with suppliers for addressing observations from audits.
Negotiate, draft, and manage quality technical agreements (QTA) and/or contracts with suppliers, ensuring alignment with internal standards, regulations, and industry standards.
Lead meetings for alignment, communication, and resolution of issues.
Ensure appropriate escalation to responsible management in case of critical findings and support immediate follow-up measures according to RevMed procedures.
Lead supplier performance metrics to monitor the health of systems, drive proactive identification of risk, and mitigate compliance issues.
Generate slides and presentations for reviews and communication to stakeholders.
Update Veeva, track KPIs, assure GxP audits.
Maintain the approved GxP supplier list and the annual audit schedules.
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.
What you need
Required Skills, Experience and Education
BA/BS degree in Biological Sciences, Chemistry, or related field and/or equivalent experience and education.
Minimum experience required 8+ years of pharmaceutical/Biotech experience with a minimum of 5+ years’ GMP Lead Auditor experience.
5 years of QTA and Supplier Quality Management experience.
ASQ Certified Quality Auditor or equivalent certifications.
Excellent leadership and people management/development skills as required.
Direct experience working with Quality System electronic databases.
Strong written and oral communication skills as well as negotiation skills.
Ability to travel occasionally (up to 25%) to perform external audits.
Flexible, and an ability to navigate through rapid growth and adapt to rapid change.
Proficiency with Microsoft Office (Excel, Outlook, PowerPoint, Word) required.
Preferred Skillsnice to have
Direct experience writing and negotiating Quality Agreements with Suppliers and partners.
Vendor Qualification and risk assessment experience.
Strategic thinking, and project management skills.
Extensive experience leading audits, evaluating CAPA and developing presentations analyzing complex data.
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Base Pay Salary Range
$164,000—$205,000 USD
Pay and benefits
$164,000 – $205,000 a year
Employer providedCompetitive cash compensation
Equity awards
Strong benefits
Learning and development opportunities
Where you'll work
Redwood City, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Redwood City, CAEqual opportunity, accessibility and legal noticesRevolution Medicines's statements, word for word
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact [email protected].
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to [email protected] so we can share these impersonations with our IT team for tracking and awareness.
Job intelligence
The context around this role
Live data · October 23, 2026
Salary intelligence
How the pay compares
This role's midpoint is 21% above the US median for Quality Assurance roles at this level.
This roleEmployer provided
Manager roles in California25 roles publishing pay
Manager roles in the US111 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $164,000 | — | $205,000 |
| California (middle half) | $158,000 | $165,500 | $181,000 |
| All US (middle half) | $132,000 | $153,000 | $167,500 |
This role: Revolution Medicines's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 23, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 927 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Revolution Medicines's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 39 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance16
- Quality systems and risk12
- Collaboration and leadership11
- Documentation and SOPs4
- Data and digital systems3
- Investigations and CAPA1
- Validation and qualification1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Revolution Medicines on Regulatory Jobs
- 17
- Open roles
- 15
- Distinct roles
- 2
- Locations
By discipline
- Quality9 53%
- Regulatory7 41%
- Compliance & Safety1 6%
By level
- Director13 76%
- Manager4 24%
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Senior QA Manager, GMP GxP Auditing & Vendor Management at Revolution Medicines
Open until filled. $164K–$205K a year, employer provided.