Avecia Pharma
QA Batch Records Specialist II – Raw Materials
Avecia Pharma, Milford, Connecticut, United States, 06466
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