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Process Lead I
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- The Process Lead participates in the manufacture of Leukocyte Interleukin, Injection (LI) under cGMP for clinical application, and facilities operations and maintenance.
- Understanding and awareness of current Good Manufacturing Practices (cGMP) and basic familiarity with FDA and EU Guidelines
- Able to follow Master Batch Record when performing LI manufacture process steps
- Demonstrates good aseptic technique and ability to work in a biological safety cabinet
- Participate in required safety, GMP, and technical training sessions
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