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QC Raw Materials Sr. Analyst I
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- This will be the largest end-to-end cell culture CDMO provider in North America.
- The new site will offer end-to-end solutionsto our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services.
- About This Role The QC Raw Materials Sr. Analyst 1 is accountable for GMP compliant laboratory operations according to USP/EP/JP regulations.
- The role will be responsible for participating in the Technology Transfer of established methods into the FDBN Quality Control Laboratory.
- Following Tech-Transfer Activities, the position will be responsible for performing raw material testing and disposition using the established analytical methods.
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