Biopharma QC Supervisor: Lead Lab Operations & Compliance

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

Benefits offered by this job

Health, Dental, and Vision Insurance

401(k) Matching

Paid Time Off

Job summary

BioTalent seeks a Quality Control Supervisor to lead daily QC operations in a biopharmaceutical setting, coordinating external testing and sample testing schedules. The role requires mentoring QC staff and partnering with Manufacturing, QA, and external clients to ensure regulatory readiness.

Candidate should hold a B.S. in a scientific discipline with 2+ years in life sciences QC/analytical labs, including 1 year in supervision; strong GMP/report-writing experience is essential.

Qualifications

• B.S. degree in a scientific discipline with 2+ years in QC/analytical lab; includes 1 year supervisory experience.
• Experience writing reports, procedures, GMPs, and regulatory audits.
• Hands-on experience with Quality Control, Lot Release, and related programs.

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.
• Collaborate with Manufacturing, QA, AD, PD, and external clients.
• Lead investigations involving OOS and OOT results.
• Support cGMP compliance, regulatory readiness, and continuous improvement initiatives.

Skills

Supervisory experience

Education

B.S. degree in a scientific discipline

Job description

BioTalent seeks a Quality Control Supervisor to lead daily QC operations in a biopharmaceutical setting, coordinating external testing and sample testing schedules. The role requires mentoring QC staff and partnering with Manufacturing, QA, and external clients to ensure regulatory readiness.

Candidate should hold a B.S. in a scientific discipline with 2+ years in life sciences QC/analytical labs, including 1 year in supervision; strong GMP/report-writing experience is essential.