Director, GLP Quality Assurance
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 GLP Quality Assurance to oversee compliance with Good Laboratory Practice standards across the company and contracted vendors. The role involves managing vendor audits, developing quality agreements, monitoring regulatory adherence, and advising internal teams on compliance matters related to nonclinical studies.
What they're looking for
- Bachelor's or Master's degree
- 12+ years of experience in global GLP Quality Assurance
- Extensive audit and inspection management experience
- Registered Quality Assurance Professional – Good Laboratory Practice (RQAP-GLP) preferred
- Planning and scheduling expertise preferred
What you'll be doing
- Ensure GLP compliance at Revolution Medicines and external contracted vendors performing regulated work
- Develop annual vendor audit plans, conduct audits, and manage closure of observations
- Perform and oversee internal audits; provide vendor approval recommendations
- Review CRO study protocols and reports for regulatory compliance using risk-based approach
- Provide GLP training to internal teams and consult with vendor QA departments on compliance issues
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.