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Gmp Compliance Jobs (NOW HIRING)

Medasource

GMP Compliance Investigator

Durham, NC · On-site

GMP Compliance Investigator - Equipment & Facilities Overview Our client is seeking a GMP Compliance Investigator - Equipment & Facilities to support a GMP manufacturing laboratory focused on ...

The Mint Dispensary

GMP Compliance Specialist

Murdock, FL · On-site

$55K - $60K/yr

This role supports the company's Compliance team by overseeing GMP adherence, managing supplier quality documentation, and assisting with BioTrack reporting. The ideal candidate is detail-oriented ...

WuXi Biologics

US GMP Compliance Head

Cranbury, NJ · On-site

$160K - $260K/yr

Job Title - US GMP Compliance Head Department - Quality Assurance Work Location - Cranbury NJ (On-site) Job Summary Reporting to QA Head of US & APAC, the US GMP compliance head will play a pivotal ...

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Gmp Compliance information

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$31.5K

$98.9K

$207.5K

How much do gmp compliance jobs pay per year?

As of Aug 30, 2026, the average yearly pay for gmp compliance in the United States is $98,949.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $115,000.00 per year, depending on experience, location, and employer.

What is GMP compliance?

GMP compliance refers to adhering to Good Manufacturing Practice (GMP) regulations, which are guidelines set by agencies like the FDA to ensure products are consistently produced and controlled according to quality standards. These practices cover all aspects of manufacturing, from raw materials to hygiene and staff training. GMP compliance is critical in industries such as pharmaceuticals, food, and cosmetics to ensure product safety and efficacy. Regular audits, documentation, and continuous improvement are essential parts of maintaining GMP compliance.

What are some common challenges faced by professionals working in GMP compliance roles?

Professionals in GMP (Good Manufacturing Practice) compliance often encounter challenges such as keeping up with evolving regulatory requirements, ensuring consistent implementation of procedures across all departments, and managing detailed documentation. They also work to foster a culture of quality and compliance among teams that may have varying levels of GMP knowledge. Additionally, GMP compliance specialists frequently collaborate with production, quality assurance, and regulatory affairs teams to coordinate audits, resolve non-conformities, and support continuous improvement efforts.

What are the key skills and qualifications needed to thrive as a GMP compliance professional, and why are they important?

To thrive as a GMP Compliance professional, you need a strong understanding of Good Manufacturing Practices, regulatory guidelines, and quality assurance, typically supported by a degree in life sciences or a related field. Familiarity with quality management systems (QMS), audit processes, and relevant certifications such as Six Sigma or ISO standards is highly valued. Attention to detail, strong analytical thinking, and effective communication are essential soft skills for this role. These abilities ensure that manufacturing processes consistently meet regulatory requirements, safeguarding product quality and organizational reputation.

What is the difference between Gmp Compliance vs Quality Assurance Specialist?

AspectGmp ComplianceQuality Assurance Specialist
CertificationsGMP Certification, Regulatory Compliance TrainingISO 9001, Quality Management System Training
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingManufacturing, healthcare, or pharmaceutical industries
Employer & Industry UsageRegulatory agencies, pharmaceutical companiesManufacturers, quality departments

Gmp Compliance focuses on ensuring products meet Good Manufacturing Practice standards and regulatory requirements. Quality Assurance Specialists oversee overall quality systems, including GMP adherence, but also broader quality processes. While both roles require knowledge of GMP, Gmp Compliance is more specialized in regulatory adherence, whereas Quality Assurance covers a wider scope of quality management.

Who is responsible for GMP compliance?

GMP compliance is primarily the responsibility of quality assurance and quality control teams within a company, with oversight from management. These professionals ensure manufacturing processes meet regulatory standards through audits, documentation, and training, often requiring knowledge of Good Manufacturing Practices and relevant certifications.
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What are the most commonly searched types of Gmp Compliance jobs?

The most popular types of Gmp Compliance jobs are:

What states have the most Gmp Compliance jobs?

States with the most job openings for Gmp Compliance jobs include:

What job categories do people searching Gmp Compliance jobs look for?

The top searched job categories for Gmp Compliance jobs are:

Gmp Compliance jobs near you
Infographic showing various Gmp Compliance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $98,949 per year, or $47.6 per hour.

GMP Compliance Investigator

Durham, NC • On-site

Medasource
Health Care and Social Assistance • 201 - 500 employees
Learn more about Medasourceexternal

Contractor

Posted 18 days ago

Job description

GMP Compliance Investigator - Equipment & Facilities
Overview
Our client is seeking a GMP Compliance Investigator - Equipment & Facilities to support a GMP manufacturing laboratory focused on advanced cellular therapies. This individual will play a key role in maintaining compliance with FDA regulations and applicable accreditation standards by leading investigations, authoring quality documentation, and partnering closely with Manufacturing and Quality teams.
This is a highly collaborative role for someone with strong GMP quality experience, exceptional technical writing skills, and the ability to manage complex investigations from initiation through closure.
Responsibilities
  • Develop, revise, and maintain Standard Operating Procedures (SOPs) to ensure compliance with FDA and applicable regulatory requirements.
  • Author and manage change controls related to SOP updates and manufacturing process improvements.
  • Edit batch records and manufacturing documentation as needed.
  • Initiate, investigate, author, and close deviations, CAPAs, investigations, and quality memos.
  • Partner with Manufacturing and Quality teams to investigate manufacturing events and drive timely closure of quality records.
  • Serve as the primary author for equipment and facility-related deviation investigations.
  • Attend meetings with equipment vendors and internal stakeholders to gather information supporting investigations.
  • Author validation documentation, including IQ, OQ, and PQ protocols, equipment assessments, and validation reports.
  • Manage deviation, CAPA, and change control timelines to support on-time batch release.
  • Perform failure mode analysis and root cause investigations.
  • Support batch release activities from a compliance perspective.
  • Ensure compliance with FDA regulations and applicable accreditation standards.
  • Train and educate personnel on updated procedures, SOPs, quality systems, and compliance requirements.
  • Assist during FDA, accreditation, sponsor, and regulatory inspections, including responses to audit observations.
  • Monitor Quality Agreements to ensure sponsor notification requirements are met.
  • Participate in continuous improvement initiatives to optimize quality systems and documentation processes.
Preferred Qualifications
  • Experience working in a Quality Assurance or GMP Compliance function within an FDA-regulated manufacturing environment.
  • Experience supporting deviations, investigations, CAPAs, and change controls.
  • Strong technical writing skills with experience authoring investigation reports and SOPs.
  • Experience participating in FDA inspections, regulatory audits, and sponsor audits.
  • Experience with electronic Quality Management Systems (QMS).
  • Project management experience.
  • Strong analytical and root cause investigation skills.
  • Excellent written and verbal communication skills.
  • Strong organizational skills with exceptional attention to detail.
  • Ability to work independently while collaborating effectively across cross-functional teams.
Minimum Qualifications
Education
  • Bachelor's degree in Biology, Life Sciences, or a related scientific discipline.

Experience
  • Minimum of 6 years of Quality Assurance, Quality Systems, or GMP Compliance experience within a regulated manufacturing environment.
  • A Master's degree in a related field may substitute for two years of experience.

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