Director, Glp Quality Assurance

Revolution Medicines

Redwood City, California, United States
Base: $211,000 - $264,000 usd; bonus/equity: compe...
On-site
12+ years glp quality assurance experience
Extensive audit and inspection management
Knowledge of 21cfr part 58 good laboratory practice
Revolution Medicines is seeking a Director of GLP Quality Assurance to ensure compliance with Good Laboratory Practices at their Redwood City location. The ideal candidate will have extensive experience in GLP QA, vendor audits, and regulatory compliance in a clinical research environment

Job Summary

  • The role involves ensuring Good Laboratory Practices compliance at Revolution Medicines and all external vendors performing regulated work.
  • Responsibilities include developing annual vendor audit plans, conducting audits, and managing the closure of observation tasks.
  • The position requires advising on compliance requirements for test articles and providing consultative guidance on computerized systems supporting GLP studies.

Matching Summary

Match Score: 85

Revolution Medicines is seeking a Director of GLP Quality Assurance to ensure compliance with Good Laboratory Practices at their Redwood City location. The ideal candidate will have extensive experience in GLP QA, vendor audits, and regulatory compliance in a clinical research environment.

Salary

Base: $211,000 - $264,000 USD; Bonus/Equity: Competitive equity awards included; Benefits: Robust benefits and learning opportunities

Skills & Requirements

Must-have

  • 12+ years GLP Quality Assurance experience
  • Extensive audit and inspection management
  • Knowledge of 21CFR Part 58 Good Laboratory Practice
  • Experience with OECD GLP Standards
  • Ability to manage external vendor audits

Nice-to-have

  • Registered Quality Assurance Professional GLP certification
  • Experience with AI and Machine Learning in biomarker labs
  • Proactive risk identification and mitigation skills
  • Effective communication with senior leadership
  • Strategic oversight balanced with detail execution

Key Requirements

  • Bachelor's or Master's Degree required
  • 12+ years global GLP QA experience
  • RQAP-GLP certification preferred
  • Expertise in 21 CFR Part 11 and ICH E6 guidelines

Work Rights

Not specified

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