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Contract Gmp Manufacturing Jobs (NOW HIRING)

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

Contract Compensation: $18.00 - $25.00 hourly Overview The Manufacturing Associate I participates ... This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ...

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

Contract Compensation: $18.00 - $25.00 hourly Overview The Manufacturing Associate I participates ... This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ...

GeneFab

Senior Manufacturing Engineer

Alameda, CA · On-site

$72 - $86/hr

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 ...

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Contract Gmp Manufacturing information

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How much do contract gmp manufacturing jobs pay per hour?

As of Sep 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 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 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 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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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:

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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 90% Full Time, 4% Part Time, 3% 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.

Biopharm Manufacturing Associate (Entry Level)

Alphanumeric

King Of Prussia, PA • On-site

$22 - $23/hr

Contractor

Re-posted 16 days ago

Job description

Biopharm Manufacturing Associate (Entry Level)

King of Prussia, PA (Upper Merion)


Alphanumeric is hiring a Biopharm Manufacturing Associate to join our client of over 20 years, a global biopharmaceutical leader dedicated to developing life-changing medicines and improving patient lives.


Pay Rate: $22.00-$23.00/hour

Launch Your Career in Biopharmaceutical Manufacturing

Are you a recent science graduate looking to break into the pharmaceutical industry? This is an excellent opportunity to gain hands-on experience in a GMP-regulated manufacturing environment while working alongside experienced professionals supporting the production of innovative therapies.

No prior pharmaceutical manufacturing experience is required-just a strong scientific foundation, attention to detail, and a willingness to learn.

What You'll Do

As a Biopharm Manufacturing Associate, you'll support daily manufacturing operations while ensuring products are produced safely, accurately, and in compliance with GMP regulations.


Responsibilities include:

  • Execute daily manufacturing activities by following Standard Operating Procedures (SOPs) and batch records.
  • Accurately document manufacturing activities in accordance with GMP requirements.
  • Dispense both small and large quantities of raw materials.
  • Perform Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) of manufacturing equipment and product tanks.
  • Assist with troubleshooting equipment and manufacturing processes.
  • Author, revise, and support SOPs, deviations, and change controls.
  • Operate within a highly regulated GMP manufacturing environment while maintaining quality and compliance standards.
  • Safely handle hazardous materials using established safety procedures.
  • Support continuous improvement initiatives and collaborate across cross-functional teams.
  • Perform additional manufacturing duties as assigned.

What We're Looking ForRequired Qualifications
  • Bachelor's degree in Biology, Chemistry, Chemical Engineering, or another scientific or engineering discipline
  • Familiarity with Good Manufacturing Practices (GMP)
  • Strong written communication and documentation skills
  • Computer proficiency
  • Ability to follow detailed written procedures
  • Strong problem-solving and troubleshooting abilities
  • Ability to work effectively in a collaborative, fast-paced environment
Preferred Qualifications
  • 1+ year of cGMP or pharmaceutical manufacturing experience
  • Knowledge of GMP regulations and documentation practices
  • Experience with upstream manufacturing processes, including media preparation and bioprocess unit operations
  • Familiarity with analytical equipment such as:
    • Vi-Cell
    • NOVA Analyzer
    • Centrifuges
    • Tubing Welders
  • Exposure to PLC, DCS, or HMI systems

Work Environment & Additional Information
  • 100% onsite position based in King of Prussia (Upper Merion), PA
  • Initial 12-month contract with the potential to extend up to 18 months based on business needs and performance
  • This is an Upstream Manufacturing role supporting biopharmaceutical production
  • Candidates must be able to wear a Powered Air-Purifying Respirator (PAPR) as required for the position
  • Following hire, candidates will complete a medical clearance/respirator screening in accordance with OSHA requirements before using a PAPR (Non-SCBA)

Why Join Us?
  • Entry point into the pharmaceutical and biotechnology industry
  • Hands-on GMP manufacturing experience
  • Work with an industry-leading global biopharmaceutical company
  • Collaborative, team-oriented environment
  • Opportunity to develop valuable technical and manufacturing skills
  • Potential for long-term career growth within biopharmaceutical manufacturing

Excellent opportunity to gain hands-on upstream biopharmaceutical manufacturing experience with a global pharmaceutical leader.


If you're passionate about science and ready to launch your career in pharmaceutical manufacturing, we'd love to hear from you!

Education:Employment Type: CONTRACTOR

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