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Gcp Quality Manager Jobs (NOW HIRING)

Senior Manager, GCP Quality Assurance page is loaded## Senior Manager, GCP Quality Assurancelocations: PA - Pennsylvania - Remotetime type: Full timeposted on: Posted Todayjob requisition id: JR ...

$165K - $207K/yr

Position Summary The Director, GCP Quality Assurance is responsible for leading Good Clinical ... Manage the internal GCP audit program, including audit planning, execution, follow-up activities ...

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Gcp Quality Manager information

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How much do gcp quality manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for gcp quality manager in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Gcp Quality Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

GCP Quality Assurance Manager at Alameda, CA 94502

Alameda, CA โ€ข On-site

$80 - $95/hr

Contractor

Re-posted 19 days ago


Job description

Job Details:

Job Title: GCP Quality Assurance Manager

Job Duration: 06 Months Contract with extension or FT conversion for local candidates

Job location: Alameda California 94502 (Fully Onsite)

Client: Exelixis, Inc. 

Join a growing clinical development organization seeking an experienced GCP Quality Assurance professional to support global clinical trials, inspection readiness, and quality oversight activities.

What You'll Do
  • Lead and execute GCP audits of investigator sites, CROs, vendors, and internal processes
  • Support inspection readiness and regulatory authority inspections
  • Review audit findings, deviations, and CAPAs
  • Partner with Clinical Operations and study teams to ensure GCP compliance
  • Provide quality guidance and identify compliance risks and improvement opportunities
What We're Looking For
  • 5+ years of GCP Quality Assurance experience in biotech, pharma, or clinical research
  • Hands-on experience conducting investigator site, CRO, and vendor audits
  • Strong knowledge of ICH E6(R3), FDA GCP regulations, and global clinical compliance requirements
  • Experience supporting inspection readiness and regulatory inspections
  • Strong communication, audit, and stakeholder management skills
Preferred
  • Oncology or biotech clinical trial experience
  • Experience with risk-based quality management and vendor oversight