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Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Senior Counsel - Pharmaceutical Development and Manufacturing

Legal Counsel & Legal SupportConfirmed live in the last 24 hours
Full-timeRedwood City, CA, USA

About the Job

Requirements

  • A J.D. from an accredited law school.
  • An active license to practice law in at least one U.S. jurisdiction.
  • At least 10 years of relevant legal experience, with significant focus on contract manufacturing or supply chain agreements.
  • Experience in the biotech, pharmaceutical, or life sciences industries, either in-house or at a law firm.
  • A strong understanding of Good Manufacturing Practices (GMP) manufacturing and regulated environments.
  • Demonstrated ability to independently negotiate complex commercial agreements.
  • Excellent communication and collaboration skills.

Responsibilities

  • Draft, review, and negotiate manufacturing-related agreements, including CDMO master services agreements and work orders; manufacturing and supply agreements; quality agreements in coordination with Quality teams; technology transfer and validation agreements; development, clinical, and commercial supply agreements; and amendments, change orders, and statements of work.
  • Advise internal stakeholders on legal, regulatory, and risk considerations related to GMP manufacturing, supply continuity, capacity planning, and technology transfers.
  • Partner with Technical Operations, Quality, Supply Chain, CMC, Finance, and Procurement teams to structure contracts that align with business and regulatory needs.
  • Identify and manage legal risks related to manufacturing, including intellectual property ownership, confidentiality, liability, indemnification, audit rights, and termination scenarios.
  • Support vendor disputes, performance issues, and contract interpretation matters.
  • Help develop and improve contracting templates, playbooks, and internal processes for manufacturing and supply agreements.
  • Stay current on industry trends, regulatory expectations, and best practices related to contract manufacturing in the biotech and pharmaceutical industries.

Desired Qualifications

  • In-house experience at a biotech or pharmaceutical company.
  • Experience supporting clinical-stage and/or commercial manufacturing.
  • Familiarity with global manufacturing arrangements and international vendors.
  • Experience working cross-functionally with technical and scientific teams.

About the Company

Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Revolution Medicines develops precision oncology drugs focused on cancers driven by RAS mutations. Its RAS(ON) inhibitors are small molecules that bind the active form of RAS to block cancer signaling, with candidates like Daraxonrasib (RMC-6236), Elironrasib (RMC-6291), and Zoldonrasib (RMC-9805) advancing in global Phase 3 trials. The company funds its research through collaborations, royalties, and upfront funding, and has not yet marketed a product. Its goal is to bring effective RAS-targeted therapies to patients and advance multiple candidates through late-stage trials toward approval, supported by strong cash reserves.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Redwood City, CA
Founded
2014

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