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Contract Gmp Manufacturing Jobs (NOW HIRING)

Recruits Lab

Quality Engineer

Phillipsburg, NJ

$36.06 - $43.27/hr

Quality Engineer (Contract) - GMP / ISO Environment Location: Phillipsburg, NJ (100% Onsite ... ASAP Overview Our client, a leading organization in regulated manufacturing, is seeking a Quality ...

Digital Prospectors

Technical Writer

Houston, TX

Technical Writer- GMP Manufacturing Documentation Location: Houston, TX (100% On-Site) Length: 6 Month Contract Please no agencies. Direct employees currently authorized to work in the United States ...

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 · 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.

Pioneer Data Systems

Scientist

South San Francisco, CA · On-site

Job Title: ScientistDuration: 18 months contract, extendable up to 24 months Location: San ... GMP manufacturing and release at a CMO. This position will also contribute to the development of ...

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

Senior Process Engineer, MSAT

Alameda, CA

$117K - $152K/yr

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 ...

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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 14, 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.

Quality Engineer

Recruits Lab

Phillipsburg, NJ

$36.06 - $43.27/hr

Contractor

Posted 21 days ago

Job description

Quality Engineer (Contract) – GMP / ISO Environment

Location: Phillipsburg, NJ (100% Onsite)

Schedule: Monday–Friday, 8:00 AM – 5:00 PM (flexible)

Duration: Up to 18 months (contract)

Compensation: $36.06–$43.27/hour (based on experience)

Start Date: ASAP


Overview

Our client, a leading organization in regulated manufacturing, is seeking a Quality Engineer to support site-level quality assurance programs and continuous improvement initiatives. This individual will play a critical role in ensuring compliance with cGMP, ISO standards, and regulatory requirements, while partnering cross-functionally to drive quality performance and operational excellence.


Key Responsibilities

  • Lead and support Quality Management System (QMS) initiatives to ensure compliance with GMP and ISO requirements
  • Drive customer complaint investigations, working directly with customers and suppliers to resolve issues
  • Manage and participate in internal, customer, and regulatory audits, including gap assessments and corrective actions
  • Own and maintain CAPA (Corrective and Preventive Action) processes within assigned scope
  • Ensure ongoing cGMP compliance and identify opportunities for process and system improvements
  • Deliver GMP/GDP training to site personnel
  • Monitor and improve quality metrics, including complaint response times and CAPA effectiveness
  • Support Change Control (Management of Change) processes
  • Conduct statistical analysis and process trending (SPC) to support data-driven decisions
  • Lead or support validation activities for new and existing products/processes
  • Collaborate with supplier quality teams to resolve material and performance issues
  • Partner with operations, R&D, procurement, and commercial teams to address quality concerns
  • Support cross-functional investigations into product and process deviations


Qualifications

  • Bachelor’s degree in Chemistry or related scientific field
  • 5+ years of experience in quality engineering or related role
  • Experience in pharmaceutical, biotechnology, or chemical manufacturing environments
  • Strong knowledge of cGMP and ISO 9000 standards
  • Minimum 3+ years in a GMP-regulated manufacturing facility


Key Skills & Competencies

  • Strong analytical and problem-solving abilities
  • Excellent written and verbal communication skills
  • Experience with quality systems: CAPA, audits, validation, complaint handling
  • Familiarity with chemical nomenclature and QC testing methods
  • Ability to work effectively in a matrixed, cross-functional environment
  • Strong project management and organizational skills
  • Proven ability to influence and lead without direct authority


Work Environment

  • Manufacturing setting requiring appropriate PPE in designated areas
  • Occasional domestic travel may be required


Interview Process

  • Initial 15-minute virtual interview
  • Final onsite interview (approximately 2 hours) with cross-functional team