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Gmp Compliance Jobs (NOW HIRING)

SBM Management Services LP

GMP Coordinator

Apex, NC · On-site

$26 - $29/hr

Oversee GMP compliance within cleaning, disinfectant, safety equipment inspections, and pertinent tasks utilizing the client's Computerized Maintenance Management System (CMMS) * Assist with ...

SBM Management Services LP

GMP Coordinator

Apex, NC

$29/hr

Oversee GMP compliance within cleaning, disinfectant, safety equipment inspections, and pertinent tasks utilizing the client's Computerized Maintenance Management System (CMMS) * Assist with ...

Cayman

QC Chemist I, GMP

Ann Arbor, MI · On-site

Maintain complete, legible, accurate, and contemporaneous records of all laboratory activities in notebooks, logbooks, and electronic systems in compliance with GMP requirements and data integrity ...

Careers at RK Pharma Inc.

GMP Cleaning

Pearl River, NY · On-site

$18 - $22/hr

This role is essential to maintaining compliance and quality standards in a cGMP environment . If ... Perform GMP-compliant cleaning throughout the facility * Clean and sanitize cleanrooms, equipment ...

Avantor Inc.

GMP Coordinator

Spring House, PA · On-site

$23 - $24/hr

GMP Compliance: Perform sanitization procedures in line with GMP standards, SOPs, and relevant procedures. * Sample Handling: Ensure proper handling of samples by transporting them in closed ...

Evotec

IT Specialist III, GMP Systems

Redmond, WA · On-site

They are seeking an IT Specialist III to drive impactful projects and support GMP systems in a manufacturing environment, ensuring compliance and effective troubleshooting of IT systems. ...

Jade Biosciences

Role Overview The Director, GMP Quality Assurance (QA) provides QA support across Jade's product ... The Director collaborates with internal and external stakeholders to support timely, compliant ...

C&W Services

GMP Cleaner

Norton, MA

$14.25 - $16.75/hr

They are expected to attain a basic understanding of GMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products ...

Lonza

LSA QA Sr. Compliance Specialist

Portsmouth, NH · On-site

$84K - $115K/yr

Serve as a subject matter expert for Quality Systems, GMP Compliance, and inspection readiness activities across the site * Lead and facilitate Quality Review Boards, including Deviation Review Board ...

Pioneer GMP Consulting

$90 - $120/hr

Cambridge/Boston, United States | Posted on 08/18/2026 Pioneer GMP Consulting is a specialized life sciences consultancy focused on delivering high-impact GMP compliance, validation, and quality ...

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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 22, 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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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 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $98,949 per year, or $47.6 per hour.

Director, QA GMP Operations

Dyne Therapeutics

Waltham, MA

Full-time

Re-posted 29 days ago

Job description

Role Summary:

The Director of QA GMP Operations is responsible for management of GMP quality within our external manufacturing operations globally and internal GMP operations for development and commercial programs. The Director will also work closely with internal business stakeholders as well as internal Quality function to deliver outcomes to advance programs within compliance.  The Director is responsible for oversight of QA activities and ensuring the quality of deliverables within the role's purview.  

This is an onsite role based in Waltham, MA.

 
Primary Responsibilities Include: 

  • Management of external quality operations in support of GMP manufacturing (clinical and commercial) activities. 
  • Manage deviations, OOS and OOTs investigations while adhering to cGMP principles and ICH guidelines. 
  • Review batch records, analytical method reports and technical reports including regulatory sections of IND/IMPD and BLA/MAAs. 
  • QA support of Tech Transfer and Process Validation activities. 
  • Disposition of GMP batches and interfacing with the Qualified Person (QP). 
  • Change management to ensure proper evaluation of manufacturing and testing related changes by Quality, Regulatory, and Subject Matter Experts. 
  • Manage CDMO performance within Quality Agreement expectations and GMP compliance.  
  • Drive continuous improvement and inspection readiness.  
  • Collaborate cross functionally to ensure pre-approval inspection and commercial readiness activities are completed at the CDMOs and internally.  
  • Adjudicate on compliance discussions and negotiate any required corrective actions. 
  • Create and foster a culture of collaboration and engagement for advancing quality outcomes and operational excellence. 

Education and Skills Requirements: 

  • Minimum of a BA/BS degree 
  • Minimum of 10+ years of experience in GMP Quality Operations in a clinical late stage and/or commercial biotechnology company 
  • Leadership experience managing cross-functional teams with an ability to influence teams to prioritize activities and allocate resources without direct authority 
  • Experience implementing and utilizing various outsourcing and support models 
  • Experience with disposition of product batches and interfacing with a Qualified Person (QP) 
  • Excellent written and oral communication skills, including well-developed presentation skills 
  • Excellent organizational skills and ability to manage multiple priorities 
  • Strong collaboration and interpersonal skills to effectively interact with internal or external stakeholders at all levels in the organization 
  • General business management knowledge to assess the impact of project decisions on financial and corporate objectives 
  • Ability to drive timelines, meet firm deadlines, and adapt quickly to changing requirements and priorities 
  • Embrace Dyne's core values and culture 

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