We are looking for an Associate I, QA Doc on behalf of our client, Biogen Idec. This position is based in Cambridge, MA...Responsibilities A temporary position to review and provide final Quality approval to Standard Operating Procedures (SOP's), Forms and Specifications. Reviews QA controlled documentation assuring accuracy and compliance to internal and GMP requirements. Enter, update and maintain required data, with a high level of accuracy, in QA computer databases. Perform ...
Veritude - 3 years ago
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