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Aseptic Manufacturing Supervisor
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- The Aseptic Supervisor Fill/Finish is responsible for supporting the overall GMP Fill Finish manufacturing processes through the application of broad knowledge of theories, techniques, and principles utilized to solve operational and routine tasks in the aseptic production of finished drug product biologics for Phase I/II & commercial GMP manufacturing.
- Ensure cGMP compliance and all its related elements in documentation, reports, and records.
- B.S. in Engineering or Science discipline and a minimum of 5-8 years of experience in biopharmaceutical based GMP manufacturing operations, related technical field, or equivalent industry experience.
- Experience with GMP fill finish operations and sound understanding of the drug development process.
- Aseptic Filling or Pharmaceutical Manufacturing experience: Background in Packaging, Pharmaceutical, Bio-Pharmaceutical, and/or Medical Devices.
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