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The successful candidate may also perform other key activities such as data review, ensuring laboratory cGMP compliance is maintained, execution of technical transfer and co-validation activities, instrumentation verification/preventative maintenance, assisting with laboratory investigations, writing procedures and technical documents as required, and providing communication of business critical information to operations and Quality Control management.
Perform Quality Control testing for in-process, release, and stability in a cGMP environment. It is preferred that the candidate have analytical experience with ELISA, qPCR, and/or cell culture
It is preferred that the candidate have analytical experience with ELISA, qPCR, and/or cell culture.
cGMP, SOP
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