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Contract Gmp Manufacturing Jobs (NOW HIRING)

Kelly Services

GMP Records Specialist (Sr.)

Stafford, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

This is a senior-level contract role requiring independent execution, strong technical writing capability, and the ability to lead documentation-related improvements in a fast-paced GMP manufacturing ...

New

Pacelabs

PLS GMP Manufacturing Technician I

Norristown, PA · On-site

$22 - $28/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a full-time, onsite, GMP Manufacturing Technician (Solid Dose) position located in ... Pace Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing ...

Randstad

GMP Manufacturing Associate II

Norwood, MA

$34 - $39/hr

... for a skilled Manufacturing Associate to join an innovative, dynamic, and supportive team in ... Role Type: 6-Month Contract * Pay Rate: Up to $38.00 per hour * Target Start Date: September 7, ...

Frontage Laboratories

Manufacturing Associate

Exton, PA · On-site

  • Medical

  • Dental

  • Life

  • Retirement

Exton, PA Full Time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract ... The Manufacturing Associate will support GMP manufacturing operations, perform hands‑on ...

Astrix Inc

Process Engineer (GMP Manufacturing)

Paris, KY · On-site

$45 - $54/hr

Contract-to-Hire Fully Onsite Key Responsibilities * Provide engineering support for manufacturing operations, equipment reliability, and process performance. * Investigate production issues, perform ...

New

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

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All JobsContract Gmp Manufacturing Jobs

Contract Gmp Manufacturing information

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How much do contract gmp manufacturing jobs pay per hour?

As of Aug 16, 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.

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 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.

GMP Records Specialist (Sr.)

Kelly Services

Stafford, TX

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago

New

Job description

Kelly Scientific has an immediate opening for a GMP Documentation Specialist (Sr.) to support a state of the art cell therapy customer near Houston, TX. 
 
Job Title: GMP Records Specialist (Sr.)
Location: Stafford, TX (onsite)
Rate: Commensurate with experience
Contract Length: 12 months 
Shift: 8am-5pm | Mon-Fri
 
Position Summary/purpose
The Contract GMP Records Specialist (Senior Level) is responsible for the end-to-end management of GMP manufacturing documentation, including the review, authoring, and maintenance of batch records, SOPs, and associated technical documents. This role ensures documentation accuracy, data integrity, and compliance with cGMP and regulatory requirements to support manufacturing operations.
 
The position operates as a subject matter expert in GMP documentation, working cross-functionally with Manufacturing, Quality Assurance, and MSAT to resolve documentation issues, drive timely record completion, and improve right-first-time performance. The role also supports digital manufacturing initiatives through hands-on involvement with Manufacturing Execution Systems (MES) and/or Electronic Batch Records (EBR), including troubleshooting and continuous improvement of documentation workflows.
 
This is a senior-level contract role requiring independent execution, strong technical writing capability, and the ability to lead documentation-related improvements in a fast-paced GMP manufacturing environment.
 
  • Roles and Responsibilities of Position
    Perform end-to-end review of GMP batch records and manufacturing documentation to ensure accuracy, completeness, and cGMP compliance.
  • Drive timely resolution of documentation errors, coordinating directly with Manufacturing, QA, and MSAT.
  • Author and revise GMP documents including Master Batch Records (MBRs), Electronic Batch Records (EBRs), SOPs, and work instructions.
  • Own document changes through the change control process, including updates, impact assessment, and implementation.
  • Support execution, troubleshooting, and continuous improvement of MES/EBR systems.
  • Serve as SME for GMP documentation practices, ensuring adherence to data integrity (ALCOA+) and regulatory expectations.
  • Partner cross-functionally to resolve documentation gaps and improve right-first-time performance.
  • Maintain document tracking and support audit and inspection readiness.
  • Provide guidance to manufacturing personnel on proper documentation practices and system usage.
 
Required Qualification (Education, Experience, Knowledge, Skills)
  • Bachelor’s degree in Life Sciences, Engineering, or a related technical field.
  • 6+ years of GMP experience in pharmaceutical, biotechnology, or cell therapy manufacturing environments.
  • Extensive experience reviewing and authoring GMP documentation, including MBRs, EBRs, SOPs, and technical instructions.
  • Demonstrated ownership of document lifecycle management and change control processes.
  • Hands-on experience with MES and/or Electronic Batch Record (EBR) systems.
  • Strong knowledge of cGMP regulations, FDA expectations, and data integrity principles (ALCOA+).
  • Proven ability to work independently, manage multiple priorities, and operate in fast-paced manufacturing environments.
  • Advanced technical writing, attention to detail, and strong organizational skills.
  • Effective cross-functional communication skills with Manufacturing, QA, and MSAT.
 
Preferred Qualifications
  • Experience in cell therapy, gene therapy, or advanced biologics manufacturing.
  • Direct experience with MES/EBR platforms (e.g., Werum PAS-X, Syncade, DeltaV, or similar).
  • Familiarity with electronic Quality Management Systems (e.g., Veeva)
  • Experience supporting commercial or late-stage GMP manufacturing operations.
  • Working knowledge of deviation management, CAPA, and change control processes.
  • Experience driving continuous improvement initiatives within GMP documentation systems.
  • Exposure to regulatory inspections (FDA, EMA) and audit readiness activities.
  • Lean Manufacturing or Operational Excellence experience.
 
Ideal Candidate Profile
  • Senior GMP documentation SME with a proven track record of independently owning batch record review, authoring, and lifecycle management.
  • Hands-on MES/EBR expert capable of troubleshooting and optimizing electronic batch record workflows.
  • Highly detail-oriented with strong technical writing skills and a focus on data integrity and right-first-time execution.
  • Able to operate autonomously in fast-paced, commercial or late-stage manufacturing environments.
  • Strong cross-functional collaborator who can effectively partner with Manufacturing, QA, and MSAT.
  • Process-driven with demonstrated ability to identify gaps and implement sustainable documentation improvements
  • Comfortable supporting audits and inspections with clear, compliant, and inspection-ready documentation.

What happens next
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
 
Helping you discover what’s next in your career is what we’re all about, so let’s get to work. Apply to be Manufacturing Support Specialist today!
 
 

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.