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Avecia Pharma

QA Batch Records Specialist II – Raw Materials

Avecia Pharma, Milford, Connecticut, United States, 06466

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A leading pharmaceutical company in Connecticut is seeking a Quality Assurance Specialist II to support QA Operations. Responsibilities include reviewing raw material documentation, coordinating quality corrections, and adhering to cGMP practices. The ideal candidate should have a BS/BA in science and at least 2 years in QA or Production. The expected salary range for this position is $65,600 to $79,800 annually. #J-18808-Ljbffr