Senior Counsel, Pharmaceutical Development and Manufacturing
Revolution Medicines · Redwood City, CA
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Role summary
Revolution Medicines seeks an experienced pharmaceutical attorney to lead drafting, negotiation, and management of complex manufacturing and supply agreements with CDMOs, suppliers, and vendors. The role requires deep biotech contracting expertise, GMP regulatory knowledge, and proven ability to partner across technical and business teams.
What they're looking for
- J.D. from accredited law school and active U.S. bar license
- 10+ years legal experience focused on contract manufacturing or supply agreements
- Biotech, pharmaceutical, or life sciences industry background (in-house or law firm)
- Strong understanding of GMP manufacturing and regulated environments
- Demonstrated ability to independently negotiate complex commercial agreements
- Excellent communication and cross-functional collaboration skills
What you'll be doing
- Draft, review, and negotiate CDMO agreements, manufacturing contracts, quality agreements, and technology transfer documents
- Advise internal stakeholders on legal and regulatory risks related to GMP manufacturing and supply continuity
- Partner with Technical Operations, Quality, Supply Chain, and Finance teams to structure contracts aligned with business needs
- Identify and manage legal risks including IP ownership, confidentiality, liability, indemnification, and termination scenarios
- Develop contracting templates, playbooks, and internal processes for manufacturing and supply agreements
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.