A leading medical device company in Deerfield Beach is looking for a QA Specialist to oversee GMP operations and ensure compliance with cGMP requirements. Responsibilities include reviewing production documentation, maintaining QA presence, and supporting audits. The ideal candidate will have a BS in Engineering or Biology and at least four years of experience in pharmaceutical or medical device manufacturing. This role offers a competitive compensation package and opportunities for professional development. #J-18808-Ljbffr SHL Medical
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