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Cmc In Biotech Jobs (NOW HIRING)

Travere

Executive Director, CMC Diligence

San Diego, CA · On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

Professional experience in similar role within biotech/pharmaceutical industry, preferably ... Strong understanding of GMP requirements, CMC regulatory expectations, process validation ...

BeiGene, Inc.

Intern - Regulatory Affairs, CMC (year-round)

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Regulatory Affairs CMC Intern will support regulatory projects consistent with company goals by ... biotech * Legally authorized to work in the United States without needing sponsorship for ...

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Cmc In Biotech information

What is a CMC in biotech position?

A CMC (Chemistry, Manufacturing, and Controls) position in biotech involves overseeing the development, manufacturing, and quality control of biopharmaceutical products. Professionals in this role ensure that products meet regulatory standards and are produced consistently, often requiring knowledge of GMP regulations, process development, and analytical techniques.

What is the difference between Cmc In Biotech vs Formulation Scientist?

AspectCmc In BiotechFormulation Scientist
Required CredentialsBachelor's or Master's in Life Sciences, Good Manufacturing Practice (GMP) knowledgeBachelor's or Master's in Pharmacy, Chemistry, or related field; GMP experience
Work EnvironmentLaboratories, manufacturing facilities, regulatory settingsLaboratories, R&D departments, manufacturing units
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract manufacturing organizationsPharmaceutical companies, biotech firms, contract labs

While both roles operate within the biotech and pharmaceutical industries, Cmc In Biotech focuses on Chemistry, Manufacturing, and Controls documentation and regulatory compliance, whereas Formulation Scientists primarily develop and optimize drug formulations. Cmc In Biotech professionals ensure regulatory submissions are complete, while Formulation Scientists work on creating effective drug delivery systems. Both roles often collaborate but serve distinct functions within the product development pipeline.

What is a CMC in biotech?

In biotech, CMC stands for Chemistry, Manufacturing, and Controls, which refers to the detailed documentation and processes involved in developing and producing a pharmaceutical product. CMC professionals ensure that manufacturing processes meet quality standards and regulatory requirements, often working with laboratory analysis, process validation, and compliance documentation.

What is the CMC department in biotech?

The CMC (Chemistry, Manufacturing, and Controls) department in biotech is responsible for developing, manufacturing, and ensuring the quality of biopharmaceutical products. It involves activities such as process development, validation, regulatory documentation, and quality control to ensure products meet safety and efficacy standards.
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Infographic showing various Cmc In Biotech job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 90% Full Time, 1% Part Time, 1% Temporary, and 6% Contract. Highlights an 80% Physical, 4% Hybrid, and 16% Remote job distribution.

Senior Counsel, Pharmaceutical Development and Manufacturing

Revolution Medicines

Redwood City, CA • Hybrid

$170K - $232K/yr

Full-time

Re-posted yesterday

Job description

The Opportunity:

RevMed is seeking an experienced attorney to support our global manufacturing, supply chain, and technical operations activities. This role will lead the drafting, negotiation, and management of complex agreements with contract development and manufacturing organizations (CDMOs), raw material suppliers, and other third-party vendors critical to drug development and commercialization.

The ideal candidate has deep experience in biotech or pharmaceutical contracting, a strong understanding of GMP and regulatory considerations, and the ability to partner effectively with business, technical, and quality teams.

A successful candidate will bring proven experience working at a publicly traded life sciences organization, with demonstrated success in driving legal cross-functional strategy.
Your Contributions (include, But Are Not Limited To)

  • Draft, review, and negotiate a wide range of 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

    • 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 tech transfers.

  • Partner closely 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 IP 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/pharmaceutical industry.

Required Skills, Experience and Education: 

  • J.D. from an accredited law school.

  • Active license to practice law in at least one U.S. jurisdiction.

  • 10+ years of relevant legal experience, with significant focus on contract manufacturing or supply chain agreements.

  • Experience in biotech, pharmaceutical, or life sciences industries (in-house or at a law firm).

  • Strong understanding of GMP manufacturing and regulated environments.

  • Demonstrated ability to independently negotiate complex commercial agreements.

  • Excellent communication and collaboration skills.

Preferred Skills:

  • 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. 

    #LI-Hybrid #LI-TS1 

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