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Quality Control Supervisor

Job in Tustin, Orange County, California, 92681, USA
Listing for: BioTalent
Full Time position
Listed on 2026-09-14
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 86400 - 108000 USD Yearly USD 86400.00 108000.00 YEAR
Job Description & How to Apply Below

Help Ensure Quality in Life-Saving Biopharmaceuticals

Are you passionate about Quality Control
, laboratory operations, team leadership, and GMP compliance? We’re looking for a Quality Control (QC) Supervisor to join a growing biopharmaceutical team supporting innovative biologic therapies.

If you thrive in a fast-paced QC laboratory environment and enjoy leading teams, managing external testing programs, and collaborating with clients and cross-functional groups, this could be your next opportunity.

What You’ll Do
  • Lead and supervise day-to-day Quality Control operations and external testing activities
  • Coordinate lot release, stability, and project sample testing activities
  • Support contract laboratory management, sample submissions, and testing schedules
  • Review and approve purchase requests, invoices, and laboratory documentation
  • Manage inventory, sample disposition, retention programs, and laboratory support functions
  • Monitor departmental performance and support achievement of business objectives
  • Train, mentor, and develop Quality Control personnel
  • Collaborate with Manufacturing, Quality Assurance, Analytical Development, Product Development, and external clients
  • Lead investigations involving out-of-specification (OOS) and out-of-tolerance (OOT) results
  • Support cGMP compliance, regulatory readiness, and continuous improvement initiatives
What We’re Looking For
  • B.S. degree in a scientific discipline and a minimum of 2 years of life science industry experience in a QC or analytical lab including 1 year of supervisory experience
  • Must have experience with writing reports, procedures, specifications, GMPs, and regulatory audits. Familiarity with the drug development process is required.
  • Hands‑on experience or exposure with
    :
  • Quality Control
  • Lot Release Testing
  • Stability Programs
  • OOS Investigations
  • Training and Mentoring
Bonus

Experience in Project Management is desirable.

$86,400 – $108,000 annually (depending on experience and qualifications)

Benefits
  • Health, Dental, and Vision Insurance
  • 401(k) Matching
  • Paid Time Off
Please Note

On-site in Tustin, CA

Overtime and weekend availability may be required

Applicants must already be authorized to work in the U.S.

#Biotech Jobs #Quality Control #QC Supervisor #Laboratory Management #GMP #Regulatory Compliance #Life Sciences #Biologics #Quality Control Jobs  #Analytical Testing #Drug Development #Leadership #Biopharma #Hiring #TustinCA

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