Director, Global CMC Regulatory
Revolution Medicines · Remote (United States)
Posted about 3 months ago
or apply directly on Revolution Medicines's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 102 days Revolution Medicines's roles stay open a median of 101 days
- Reposted
- No
- Salary listed
- No 0% of Revolution Medicines's roles list one
- Ghost-job risk at Revolution Medicines
- high 264 stale, 6 reposted of 264 open
- Hiring momentum
- 88 roles opened in the last 90 days ↓ down vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-11-14
Measured from postings appearing on and disappearing from Revolution Medicines's own greenhouse board since 2026-08-03. Full hiring picture for Revolution Medicines.
About this role
The Director, Global CMC Regulatory at Revolution Medicines is responsible for developing and executing global regulatory strategies for the company's product portfolio. This role involves overseeing the preparation of CMC dossiers, managing interactions with health authorities, and providing strategic leadership to the regulatory team. The position requires a deep understanding of global CMC regulations and the ability to anticipate regulatory risks while supporting business objectives.
- benefits
- 3/5
- freshness
- 1/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Revolution Medicines as an employer.
What you need
- Bachelor’s degree in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related scientific discipline
- Minimum of 15 years of experience in pharmaceutical/biotech drug development
- At least 5 years of hands-on global CMC regulatory affairs experience
- Deep expertise in CMC development for new chemical entities (NCEs) and small molecules
- Extensive experience leading global CMC regulatory strategy and global marketing approval applications
- Strong knowledge of US and international GMP regulations
Nice to have
- Advanced degree (MS or Ph.D) in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related field
- Experience supporting global commercial labeling implementation and lifecycle updates
- Prior experience in oncology product commercialization
What you get
- Base pay salary range of $201,000 — $251,000 USD
- Competitive cash compensation
- Robust equity awards
- Strong benefits
- Significant learning and development opportunities
Worth weighing
- Remote position may require flexibility in working hours due to global interactions
- No specific mention of the company's technology stack or tools used
- The role involves significant leadership responsibilities, which may not suit all candidates
Summarised from Revolution Medicines's posting. Read the full original.
Listed by Revolution Medicines on their greenhouse job board, last confirmed open on 2026-11-14. PitchMeAI is not the employer.
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