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Contract Gmp Manufacturing Jobs (NOW HIRING)

GeneFab

Senior Manufacturing Engineer

Alameda, CA · On-site

$103K - $141K/yr

The ideal candidate combines deep GMP manufacturing knowledge with hands-on experience implementing ... This position is offered as a contract engagement with eligibility for conversion to full-time ...

GeneFab

Senior Manufacturing Engineer

Alameda, CA

$103K - $141K/yr

The ideal candidate combines deep GMP manufacturing knowledge with hands-on experience implementing ... This position is offered as a contract engagement with eligibility for conversion to full-time ...

GeneFab

Senior Manufacturing Engineer

Alameda, CA

$103K - $141K/yr

The ideal candidate combines deep GMP manufacturing knowledge with hands-on experience implementing ... This position is offered as a contract engagement with eligibility for conversion to full-time ...

Kincell Bio, LLC

Manufacturing Associate I

Durham, NC · On-site

... contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and ...

Aerotek

Manufacturing Technician

Irvine, CA

$24.20 - $26.40/hr

Hands-on experience working in a GMP manufacturing environment. * Proficiency with aseptic ... Job Type & Location This is a Contract to Hire position based out of Irvine, CA. Pay and Benefits ...

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Contract Gmp Manufacturing information

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How much do contract gmp manufacturing jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for contract gmp manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What are some common challenges faced in a Contract GMP Manufacturing role, and how can they be addressed?

Professionals in Contract GMP Manufacturing often face challenges such as adapting to diverse client requirements, ensuring strict regulatory compliance, and managing tight production timelines. Successful candidates should be comfortable working in fast-paced environments where priorities may shift quickly. Collaboration with cross-functional teams—like Quality Assurance, Regulatory Affairs, and clients—is essential to navigate these challenges. Maintaining clear communication and robust documentation practices helps ensure both compliance and client satisfaction.

What is Contract GMP Manufacturing?

Contract GMP (Good Manufacturing Practice) Manufacturing refers to outsourcing the production of pharmaceutical, biotechnology, or medical device products to specialized manufacturers who comply with GMP regulations. These contract manufacturers have the facilities, expertise, and quality systems required to ensure products are consistently produced and controlled according to regulatory standards. Companies often use contract GMP manufacturers to save costs, access specialized technology, or scale production quickly without investing in their own manufacturing infrastructure.

What are the key skills and qualifications needed to thrive as a Contract GMP Manufacturing professional, and why are they important?

Success in Contract GMP Manufacturing requires a solid background in bioprocessing or pharmaceutical manufacturing, a strong understanding of Good Manufacturing Practices (GMP), and typically a degree in a relevant scientific or engineering field. Familiarity with industry-standard quality management systems, batch record documentation, and equipment validation, as well as certifications like Six Sigma or cGMP training, are highly valued. Attention to detail, problem-solving skills, and effective communication help professionals navigate regulatory requirements and collaborate with clients and cross-functional teams. These competencies ensure product quality, regulatory compliance, and client satisfaction in a highly regulated manufacturing environment.

What is the difference between Contract Gmp Manufacturing vs Quality Control Analyst?

AspectContract Gmp ManufacturingQuality Control Analyst
CertificationsGMP training, relevant manufacturing certificationsGMP, QC certifications, lab skills
Work EnvironmentManufacturing facilities, production linesLaboratories, testing environments
Industry UsagePharmaceutical manufacturing, biotechQuality assurance, testing labs

Contract Gmp Manufacturing involves producing pharmaceutical products under GMP standards, focusing on manufacturing processes. Quality Control Analysts test and verify product quality in labs. While both roles require GMP knowledge, manufacturing roles emphasize production, whereas QC analysts focus on testing and quality assurance.

More about Contract Gmp Manufacturing jobs
What cities are hiring for Contract Gmp Manufacturing jobs? Cities with the most Contract Gmp Manufacturing job openings:
What are the most commonly searched types of Gmp Manufacturing jobs? The most popular types of Gmp Manufacturing jobs are:
What states have the most Contract Gmp Manufacturing jobs? States with the most job openings for Contract Gmp Manufacturing jobs include:
What job categories do people searching Contract Gmp Manufacturing jobs look for? The top searched job categories for Contract Gmp Manufacturing jobs are:
Contract Gmp Manufacturing jobs near you
Infographic showing various Contract Gmp Manufacturing job openings in the United States as of June 2026, with employment types broken down into 40% Full Time, 20% Temporary, and 40% Contract. Highlights an 100% In-person job distribution, with an average salary of $51,890 per year, or $24.9 per hour.
Senior Counsel, Pharmaceutical Development and Manufacturing

Senior Counsel, Pharmaceutical Development and Manufacturing

Revolution Medicines

Redwood City, CA • Hybrid

$170K - $232K/yr

Other

Posted 27 days ago

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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