Senior QC Supervisor - Biopharma | On-site CA

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

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.