Medium
A leading biotechnology firm is seeking an Associate Director of Clinical Quality Assurance to ensure compliance with GMP guidelines and drive quality culture. The ideal candidate will have over 10 years of experience in the pharmaceutical industry and at least 5 years in a QA management role. Responsibilities include leading the QA department, managing budget, and ensuring compliance with regulatory standards. This position is based in Bend, Oregon, offering competitive benefits and a collaborative work environment.
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