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CGMP Specialist
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Starting at $60,000 a year
Full-time
- Description of Work Development and scale-up of purification processes to the production site for generating cGMP clinical trial material.
- Assist with production of cGMP material for Phase I/II clinical trials.
- Verify and assist with run preparations consisting of media/buffer prep, equipment calibration, and cleaning and sterilization.
- Monitor and troubleshoot engineering and cGMP production runs in the BPDF GMP suite.
- Create equipment and process validation protocols.
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