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Supervisor of Quality Control
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- The Supervisor of Quality Control is responsible for overseeing activities related to the QC testing of Leukocyte Interleukin, Injection (LI) under current Good Manufacturing Practices (cGMP) for clinical application, and facilities operations and maintenance.
- The Supervisor of Quality Control reports directly to the Manager of Quality Control.
- At least five (5) years of experience with at least 1+ years in a supervisory position of a QC laboratory in the Biotechnology, Biopharmaceutical or Pharmaceutical industry working with GMP. Specific experience should include but not be limited to: ELISA testing, Protein assays, gel-electrophoresis, particulate visual inspection, raw materials testing, and general laboratory supervision and maintenance (inventory control, equipment qualification, personnel training).
- Knowledge and practical experience with HPLC, Endotoxin (LAL), Microbial testing and Analytical Methods Validation (AMV) a plus.
- Ensure the timely testing LI cell culture supernatant, bulk solution, formulated LI drug solution and finished product (per LI Master Batch Record, MBR
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