CQV Lead: Biopharma Validation & Commissioning
Trinity Consultants
A leading engineering consultancy is seeking a CQV Lead to oversee the commissioning and qualification processes in the pharmaceutical industry. The successful candidate will have over 10 years of experience in CQV and a Bachelor's degree in Engineering or Life Sciences. Key responsibilities include developing and executing validation protocols and ensuring compliance with regulatory standards. This role requires strong communication skills and hands-on experience with biopharmaceutical equipment. The position is based in Indiana, Pennsylvania. #J-18808-Ljbffr
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