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Director Gmp Compliance Jobs (NOW HIRING)

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 ...

Cellares

Director, GMP Systems

South San Francisco, CA · On-site

$90K - $250K/yr

We are seeking a Director, GMP Systems, who will be a hands-on technology and operations leader ... Translate evolving operational needs into practical, compliant system solutions * Ensure systems ...

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 ...

Cellares

Director, GMP Systems

South San Francisco, CA · On-site

The Director, GMP Systems will be responsible for stabilizing and improving the company's critical ... into practical, compliant system solutions • Ensure systems support operational execution ...

Cellares

Director, GMP Systems

South San Francisco, CA · On-site

$90K - $250K/yr

We are seeking a Director, GMP Systems, who will be a hands-on technology and operations leader ... Translate evolving operational needs into practical, compliant system solutions * Ensure systems ...

Olema Oncology

Associate Director, GMP Quality

Boston, MA

$160K - $180K/yr

About the Role >>> Associate Director GMP Quality As the Associate Director, GMP Quality, reporting ... Supplier compliance. In this role you will also collaborate with other functional teams such CMC ...

Cellares

Director, GMP Systems

South San Francisco, CA · On-site

$90K - $250K/yr

We are seeking a Director, GMP Systems, who will be a hands-on technology and operations leader ... Translate evolving operational needs into practical, compliant system solutions * Ensure systems ...

Formation Bio

Associate Director, GMP Quality

Boston, NY · On-site

$161K - $202K/yr

About the Position The Associate Director, GMP Quality Assurance is responsible for ensuring that ... Ensure compliance with global regulations (e.g., FDA, EMA, ICH) and internal SOPs. Policies and ...

Cellares

Director, GMP Systems

South San Francisco, CA · On-site

$90 - $250/hr

We are seeking a Director, GMP Systems, who will be a hands‑on technology and operations leader ... Translate evolving operational needs into practical, compliant system solutions * Ensure systems ...

Formation Bio

Associate Director, GMP Quality

Boston, MA · On-site

$161K - $202K/yr

About the Position The Associate Director, GMP Quality Assurance is responsible for ensuring that ... Ensure compliance with global regulations (e.g., FDA, EMA, ICH) and internal SOPs. Policies and ...

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Director Gmp Compliance information

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$42.5K

$128.3K

$199.5K

How much do director gmp compliance jobs pay per year?

As of Aug 22, 2026, the average yearly pay for director gmp compliance in the United States is $128,297.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,000.00 and $145,000.00 per year, depending on experience, location, and employer.

What is the difference between Director Gmp Compliance vs Quality Assurance Manager?

AspectDirector Gmp ComplianceQuality Assurance Manager
CertificationsGMP certifications, Regulatory Affairs certificationsGMP, ISO, QA certifications
Work EnvironmentRegulatory compliance departments, corporate officesManufacturing sites, quality control labs
Employer & Industry UsagePharmaceutical, biotech, medical device companiesPharmaceutical, biotech, manufacturing companies
Primary FocusEnsuring compliance with GMP regulations and standardsOverseeing quality assurance processes and procedures

The main difference is that the Director Gmp Compliance focuses on regulatory adherence and GMP standards at a strategic level, while the Quality Assurance Manager handles day-to-day quality processes and implementation. Both roles are essential in maintaining product quality and compliance within the industry.

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Director Gmp Compliance jobs near you
Infographic showing various Director 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 $128,297 per year, or $61.7 per hour.

Director of Cranbury GMP Compliance

WuXi Biologics

Cranbury, NJ • On-site

$134K - $228K/yr

Full-time

Posted 9 days ago

Job description

Job Title: Director, GMP Technical Operations & Readiness
Location: Cranbury, NJ, USA
Department: US GMP Operations
Reports to: Head of US GMP Operations
Position Summary
The Director, GMP Technical Operations & Readiness provides scientific, technical, and GMP leadership supporting biologics Manufacturing and Quality Control operations at the Cranbury site.
This role works closely with Manufacturing, QC, Engineering, QA, MSAT, Validation, Project Management, clients, and external partners to resolve complex technical issues, support technology transfer and validation activities, strengthen GMP compliance, and prepare the site and client programs for regulatory inspections and commercial manufacturing.
Key Responsibilities
  • Provide scientific and technical leadership supporting GMP Manufacturing and QC operations, including analytical controls, product quality, troubleshooting, and operational readiness.
  • Partner with Manufacturing, QC, Engineering, QA, MSAT, and Validation to assess technical and GMP risks, resolve complex issues, and support continuous improvement.
  • Work with clients and internal SMEs to conduct PLI and regulatory inspection gap assessments, identify readiness risks, develop action plans, and support inspection preparation.
  • Support client audits and regulatory inspections through readiness assessments, facility and operational walkthroughs, SME preparation, documentation review, and technical responses.
  • Provide practical guidance to Manufacturing and QC teams on GMP compliance, investigations, documentation practices, data integrity, and regulatory expectations.
  • Support analytical method lifecycle, technology transfer, equipment/process validation, PPQ, and commercial manufacturing readiness activities.
  • Support manufacturing and laboratory investigations, deviations, OOS/OOT events, process changes, comparability assessments, and other technical issues in collaboration with QA and functional SMEs.
  • Provide technical oversight of external laboratories, CROs, CDMOs, and vendors, and contribute technical expertise to CMC documentation, regulatory submissions, and client communications.

Qualifications
  • BS, MS, or PhD in a relevant scientific or engineering discipline.
  • 12+ years of experience in biologics, pharmaceutical manufacturing, QC, Analytical Development, CMC, or Technical Operations.
  • 5+ years of leadership or management experience.
  • Strong experience supporting GMP biologics Manufacturing and/or QC operations.
  • Experience working cross-functionally with Manufacturing, QC, Engineering, QA, and Validation.
  • Experience supporting regulatory inspections, client audits, GMP gap assessments, or inspection readiness activities.
  • Experience with analytical lifecycle management, technology transfer, validation, PPQ, or commercial manufacturing readiness.
  • Experience working with clients, CROs, CDMOs, contract laboratories, or other external partners.
  • PLI/PAI readiness experience preferred.

Key Competencies
  • Strong scientific and technical judgment
  • Practical understanding of GMP operations
  • Cross-functional collaboration and influencing skills
  • Client-facing and inspection-readiness capabilities
  • Strong problem-solving and risk-assessment skills
  • Excellent communication and leadership skills

The anticipated salary range for this position is $134,400 to $228,500
Job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

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