Quality Control Supervisor

BioTalent; Tustin (CA); On-site; USD 86,000 - 108,000; Full time

Benefits offered by this job

Health, Dental, Vision Insurance

401(k) Matching

Paid Time Off

Job summary

BioTalent seeks a Quality Control Supervisor to lead day-to-day QC operations in a biopharma setting, coordinating lot release, stability, and testing schedules. You will manage external labs, review documentation, and mentor QC staff to ensure cGMP compliance and regulatory readiness.

The role requires a BS in a life sciences field with 2+ years in QC/analytical labs and at least 1 year in supervision. On-site in California, with competitive benefits.

Qualifications

• B.S. degree with 2+ years life science QC/analytical lab and 1 year in supervision.
• Experience writing reports, procedures, specifications, GMPs, and audits.
• Familiarity with the drug development process.

Responsibilities

• Lead and supervise day-to-day Quality Control operations and external testing activities.
• Coordinate lot release, stability, and project sample testing.
• 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.
• Lead investigations involving OOS and OOT results.

Skills

Quality Control

Supervisory experience

GMP compliance

Regulatory audits

Laboratory operations

Education

B.S. in a scientific discipline

Job description

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)

• 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.