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Manufacturing Supervisor, Downstream
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- Technical expertise includes Column Chromatography, tangential flow filtration, cGMP compliance, SOP development, operational/workflow efficiency, process validation and technology transfers.
- The area supervisor is responsible for the safe, compliant, and Right First Time, hands-on, and supervision of purification processing to produce clinical and commercial material that is compliant with cGMPs and meets strategic objectives.
- Processing experience includes but not limited to: Chromatography, writing/using unicorn methods, Tangential Flow Filtration, Aseptic processing, bulk drug substance and drug product operations.
- Support technology transfer and/or process development through active participation in ensuring that new processes fit and execute consistently in the cGMP space.
- B.A./B.S degree in Chemical Engineering, Biology, or similar relevant field with at least 6 years of direct GMP manufacturing experience in a biotechnology manufacturing facility or Pilot Plant OR a High School Diploma with 10 years of experience in protein purification in Biotech/Pharmaceutical industry.
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