Director, GMP QA Operations
Revolution Medicines · Redwood City, CA
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Revolution Medicines seeks a Director of GMP QA Operations to lead quality oversight for assigned clinical and commercial oncology products. The role manages GMP compliance across external manufacturing partners and suppliers, overseeing drug substance through packaged product, and ensures batch disposition and regulatory readiness.
What they're looking for
- Extensive GMP quality assurance experience in pharmaceutical manufacturing oversight
- Proven leadership in managing external CMOs, CDMOs, and supplier quality networks
- Strong knowledge of batch record review, deviation investigation, and CAPA processes
- Experience supporting regulatory submissions, health authority inspections, and product launches
- Demonstrated expertise in quality risk assessment and compliance issue resolution
- Cross-functional collaboration experience with supply chain and manufacturing teams
What you'll be doing
- Serve as primary GMP QA lead for assigned products, providing quality oversight and strategic direction
- Review batch records, testing documentation, and GMP materials; perform batch disposition decisions
- Oversee external manufacturing partners and suppliers; conduct quality assessments and trend analysis
- Lead quality interactions with external partners on expectations, risks, and release timelines
- Review and approve deviations, investigations, CAPAs, and change controls for quality events
Privacy & handoff
This role links to Revolution Medicines's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.