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Director Qc Gmp Jobs (NOW HIRING)

Revlon Corporate

Director, Quality Control

Oxford, NC · On-site

Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the Oxford, NC manufacturing site. This role is responsible for ensuring timely, accurate, compliant ...

Epoch Biodesign

Director, Quality Control

Dallas, TX · On-site

As Director of Quality Control , you will own the quality function across Crusoe's data center construction portfolio. You will set the standard -- building the systems, frameworks, and team that ...

Calibre CPA Group

Director, Quality Control

Bethesda, MD · On-site

$100K - $150K/yr

Quality Control Director will ensure accuracy, completeness, and compliance of all audit engagements. You will review audit workpapers, financial statements, and related documentation to ensure ...

Calibre CPA Group

Director, Quality Control

Bethesda, MD · On-site

$100K - $150K/yr

Quality Control Director will ensure accuracy, completeness, and compliance of all audit engagements. You will review audit workpapers, financial statements, and related documentation to ensure ...

Ott Scientific

Quality Control Analyst I

Warrington, PA · On-site

$59K - $69K/yr

Experience with quality control GMP documentation of analytical testing results and assurance of laboratory data integrity and compliance preferred. * Knowledge of analytical equipment, analytical ...

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As of Sep 11, 2026, the average yearly pay for director qc gmp in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Director Qc Gmp job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Associate Director, Quality Control

San Francisco, CA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$162K - $227K/yr

Other

Medical, Retirement, PTO

Posted 13 days ago

Job description

Associate Director, Technical Operations Quality ControlWhat You’ll Do
  • Translate and implement QC strategy for assigned programs and external testing networks (CDMOs/CTLs) aligned with QC/Quality/Technical Operations objectives.
  • Lead QC activities across the product lifecycle (Phase 1 through commercial) for multiple programs, ensuring phase-appropriate control strategies and timely analytical deliverables.
  • Develop/refine QC strategies (methods, specifications, testing approaches, and external execution models) with Analytical Development and QC leadership.
  • Drive harmonization of QC methods/specifications/practices/documentation across programs and partners.
  • Identify/escalate QC performance, supply, regulatory, and compliance risks; develop mitigation plans.
  • Represent QC on CMC/program teams; align QC deliverables and readiness for key CMC milestones.
  • Provide leadership/coaching; may manage/mentor QC colleagues and external partners.
  • Oversee QC operations for timely, compliant release/stability testing (internal and outsourced).
  • Oversee GMP documentation review (analytical data, batch records, CoAs); manage deviations, OOS/OOT, change controls, investigations, CAPAs with QA.
  • Manage CTL/CDMO performance (governance, metrics, issue resolution).
  • Oversee method lifecycle (qualification/transfer/validation/implementation/optimization/ongoing monitoring).
  • Oversee reference standards and critical QC reagents.
  • Support regulatory filings/health authority responses and serve as QC SME for audits/technical visits.
  • Drive continuous improvement across QC processes and external network performance.
Who You Are and What You Bring
  • BA/BS (12+ yrs), MA/MS/MBA (10+ yrs), or PhD (8+ yrs) in Biochemistry, Chemistry, Biology, Virology, Chemical Engineering, or related field (preferred).
  • Technical expertise in analytical methods for biologics release/stability (e.g., mAbs, recombinant proteins).
  • Strong knowledge of cGMP, ICH, FDA, and EMA; QC and/or assay development background.
  • Experience with analytical method optimization, qualification, validation, transfer, implementation, and lifecycle management.
  • Experience overseeing external partners (CDMOs/CTLs) in an outsourced model.
  • Experience supporting CMC regulatory submissions, health authority responses, audit/inspection readiness.
  • Strong communication; ability to assess risk, prioritize across programs, and execute in a matrixed environment.
Location

San Francisco headquarters; 3 days/week in office.

Compensation/Benefits
  • Expected salary range: $162,500–$227,500/year; includes compensation, bonus and equity plus benefits
  • health/welfare plans
  • non-accrual PTO
  • holiday shutdown
  • commuter benefits
  • 401K match
  • lunch in office
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