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Contract Gmp Manufacturing Jobs (NOW HIRING)

GeneFab

Senior Process Engineer, MSAT

Alameda, CA · On-site

$117K - $152K/yr

Provide technical oversight during engineering and GMP manufacturing runs to evaluate process ... a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies.

GeneFab

Bioprocess Specialist - CONTRACT

Alameda, CA · On-site

$40 - $50/hr

Work as part of a team to support the execution of daily GMP manufacturing activities. * Train ... a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies.

Pioneer Data Systems

Scientist

South San Francisco, CA · On-site

Job Title: ScientistDuration: 18 months contract, extendable up to 24 months Location: San ... Support clinical-scale non-GMP/ GMP IND-enabling manufacturing operations, including Tech Transfer ...

GeneFab

Senior Process Engineer, MSAT

Alameda, CA

$117K - $152K/yr

Provide technical oversight during engineering and GMP manufacturing runs to evaluate process ... a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies.

GeneFab

Bioprocess Specialist - CONTRACT

Alameda, CA · On-site

$40 - $50/hr

Work as part of a team to support the execution of daily GMP manufacturing activities. * Train ... About GeneFab GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell ...

GeneFab

Senior Process Engineer, MSAT

Alameda, CA · On-site

$72 - $89/hr

Provide technical oversight during engineering and GMP manufacturing runs to evaluate process ... About GeneFab GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell ...

System One

Manufacturing Associate Level II

Edison, NJ · On-site

$20/hr

Edison, NJ Type: Contract To Hire Compensation: $20.00 Work Model: Onsite Responsibilities ... Ensure compliance with Good Manufacturing Practices (GMP). * Maintain a clean and organized work ...

GeneFab

Bioprocess Specialist - CONTRACT

Alameda, CA

$40 - $50/hr

Work as part of a team to support the execution of daily GMP manufacturing activities. * Train ... a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies.

Actalent

Manufacturing Associate

Plainville, MA

$27 - $28/hr

No steel toes, but closed toed shoes, GMP environment regulations - no piercing, no polish ... is a Contract position based out of Plainville, MA. Pay and Benefits The pay range for this ...

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Contract Gmp Manufacturing information

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How much do contract gmp manufacturing jobs pay per hour?

As of Aug 15, 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?

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.

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Contract Gmp Manufacturing jobs near you
Infographic showing various Contract Gmp Manufacturing job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 4% Part Time, 4% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

Scientist

Pioneer Data Systems

South San Francisco, CA • On-site

Contractor

Re-posted 13 days ago

Job description

Company Description
Job Description
Position Details:
Job Title: ScientistDuration: 18 months contract, extendable up to 24 months
Location: San Francisco, CA
Job Description:
We are seeking a highly motivated, results-oriented, self-starter who demonstrates personal accountability for outcomes and thrives on increasing levels of responsibility, to join a new and dynamic team responsible for successful development and characterization of clinical-scale manufacturing processes for Chimeric Antigen Receptor T-cell (CART) therapies. The successful candidate will contribute to the development, implementation and characterization of state-of-the-art processing technologies to deliver scalable and robust manufacturing processes, and support successful tech transfer for GMP manufacturing and release at a CMO. This position will also contribute to the development of Client technologies and approaches to meet future CART manufacturing needs and will work in close collaboration with key stakeholders including the CART Research and Bioprocess R&D groups.
Job Responsibilities:
• Actively contribute to development, implementation, characterization and successful execution of robust, state-of-the-art CART manufacturing processes.
• Support clinical-scale non-GMP/ GMP IND-enabling manufacturing operations, including Tech Transfer to CMO and support of successful GMP manufacturing of clinical material.
• Contribute to relevant and impactful innovation programs to enhance CART manufacturing technologies/ capabilities and work-processes (such as alternate transfection/ cell engineering strategies, media development, disposable/ closed production systems and automation), aligned with emerging business drivers and Regulatory expectations.
• Contribute to Project Technical Teams and communicate and collaborate effectively to ensure effective interactions with all stakeholder groups
• Demonstrate strong "personal leadership"/ accountability and technical and interpersonal skills, and apply scientific and technical experience to ensure safe, high-quality lab practices
• Ensure high-quality, timely documentation in electronic laboratory notebooks and Technical Reports and contribute to Regulatory Filings and responses to Regulatory questions as appropriate.
• Present data/ strategy to scientists (and management) in internal venues (technical meetings, Project Team meetings) as appropriate.
Technical Skills Requirements:
BS or MS degree in Molecular Immunology/ Molecular Biology, Bioengineering, or related degree (with appropriate cell and gene therapy focus) with 3+ years (1+ for MS) of experience in biotech/biopharma industry (preferably in the development and characterization of manufacturing processes for cell- or gene-based therapies).
• Process development for GMP manufacturing of cell- or gene-therapies
• Culture and characterization of primary T-cells, T-cell molecular biology/ engineering
• Aseptic cell culture technique
• Direct experience with T-cell activation, viral transduction, and mRNA electroporation is highly desirable
• Familiarity with cGMP and relevant Regulatory Guidance documents a plus
• Familiarity with single-use bioprocessing such as WAVE bioreactors and CliniMACS Prodigy a plus
• Experience with process scale-up and scale-down is desired
• Knowledge with Design of Experiments a plus
Qualifications
Additional Information
Anuj Mehta
732-947-3452

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