# Associate Director, GMP Quality Assurance at Revolution Medicines

- Company: Revolution Medicines
- What the company does: Backed by GV.
- Type: Startups
- Level: Principal and up
- Location: Redwood City, California, United States
- Work setup: On-site
- Posted: 2026-08-17
- Apply by: 2026-10-14
- Apply: https://www.revmed.com/careers-list/?gh_jid=7887615003
- Page: https://www.1752.vc/careers/jobs/revolution-medicines-associate-director-gmp-quality-assurance/

## About the role

The Associate Director, GMP Quality Assurance will provide quality oversight and decision-making authority for development, technology transfe , manufacture, testing, and batch disposition of small molecule Drug Substance (DS) and Drug Product Intermediate (DPI). The role ensures GMP compliance, product quality, data integrity, and inspection readiness for late-stage clinical and commercial programs.

## What they're looking for

- A Bachelor's degree in a scientific or technical discipline is required
- A minimum of 10+ years of progressive GMP Quality experience, including late-stage or commercial small molecule DS and/or DPI manufacturing
- Quality oversight of CDMOs supporting technology transfer, validation/PPQ, manufacturing, testing, and batch release
- Inspection readiness experience in the United States and ex-US markets
- Technical knowledge of small molecule process chemistry, process controls, impurity management, analytical testing, specifications, and validation
- Knowledge of applicable US and global GMP regulations and industry practices

Tags: Quality Assurance

Source: 1752vc Careers, https://www.1752.vc/careers/jobs/revolution-medicines-associate-director-gmp-quality-assurance/