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Contract Gmp Manufacturing Jobs (NOW HIRING)

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 · 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 · 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 ...

Apply Early

CSBio

Chemist, GMP Production

Milpitas, CA · On-site

CSBio is a peptide contract manufacturing founded in 1993. Our initial products were a complete ... GMP Synthesis * Execute batch production records or protocols for synthesis and cleavage processes ...

Kincell Bio, LLC

Supervisor, Manufacturing

Gainesville, FL · On-site

$54K - $74K/yr

... 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 ...

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Contract Gmp Manufacturing information

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How much do contract gmp manufacturing jobs pay per hour?

As of Jul 6, 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:
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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 96% Full Time, 1% Temporary, 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.
MCS Manufacturing Senior Associate, Biopharma (JP11845)

MCS Manufacturing Senior Associate, Biopharma (JP11845)

3 Key Consulting

Thousand Oaks, CA • On-site

$32 - $37/hr

Other

Posted 16 days ago

Job description

Job Title:MCS Manufacturing Senior Associate, Biopharma (JP10845)
Location:Thousand Oaks, CA.
Employment Type: Contract
Business Unit:Manufacturing Systems
Duration:18 months
Rate: $32-37/Hr W2
Posting Date:10/03/2023
3 Key Consulting is hiringMCS(Manufacturing and Clinical Supply) Manufacturing Sr. Associatefor a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
In this vital role you will be part of the Manufacturing Systems team which is responsible for supporting manufacturing activities through new product introduction, new technology and equipment introduction, continual improvement projects, supporting the multiproduct facility operation program, CAPA ownership, and optimization/implementation of single use technologies. The position is within the drug substance supply organization in ATO Building 23 which is a dynamic environment and an important launch point for Amgen's pipeline products. The plant manufactures drug substance at all phases of clinical trials through commercial production.
Responsibilities include:
  • Support manufacturing by providing subject-matter expertise for drug substance upstream and downstream processes as process owner (PPO) or Single-use SME.
  • Lead projects using project management skills.
  • Resolve quick issues and execute function tests to troubleshoot and optimize process.
  • Write protocols and reports in support of validation, function testing, equipment commissioning and qualification, and change management.
  • Own Quality Records, such as CAPA, and CAPA-EV.
  • Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs) as instructed by the production schedule to execute function-testing and project tasks with minimal disruption to operations.
  • Available to work on site.
  • Must be able to work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work while following GMP documents (SOPs) with strict adherence to safety and compliance.
  • Apply technical process, scientific, operational, and compliance knowledge with analytical troubleshooting skills to support the implementation of new technologies into the plant.
  • Demonstrate strategic problem-solving skills and champion continual improvement.
  • As Process owner:
    o Support operational readiness of new technologies, equipment, or processes by applying technical process, scientific, operational, and compliance knowledge with project management skills
    o Develop/own drug substance manufacturing processes and procedures. Draft and revise GMP manufacturing documents (SOPs, Forms). Draft and develop user requirements for new technologies.
  • As Single-use SME:
    o Support New Product introduction and projects through SUS mapping
    o Support manufacturing and quality through the SUS defect/leak triage process - perform troubleshooting on the floor, initiate investigation and bring leaks and defects to triage
    o Initiate EN/SICAR records and follow process to conclusion, including working with vendors on investigation.
    o Maintain up-to-date EN/SICAR/EE trackers and manage or lead small to medium projects
    o Understand single-use material capabilities and user requirements for new technologies.

Basic Qualifications:
Master's degree OR
Bachelor's degree and 2 years of experience OR
Associate's degree and 6 years of experience
Top Must Have Skills:
  • Degree in Engineering or Life Sciences (if not, then at least 5 years' experience)
  • Experience in Drug substance GMP technical support roles, GMP manufacturing, Engineering, Process Development, or equivalent.
  • Ability to learn quickly, self-monitor, and prioritize.
  • Previous biopharma industry experience highly preferable

Interview process:
Webex interviews. Potential for in-person follow-up.
We invite qualified candidates to sendyour resume torecruiting@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this position, please feel free to look at the other positions on our websitewww.3keyconsulting.com/careers. You are welcome to also sharethis opportunity withanyone you think might be interested in applying for this role.

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