CQV Specialist: Packaging Systems for Biotech & Pharma

A leading engineering services company in Kentucky is seeking a CQV Specialist to support commissioning, qualification, and validation activities for packaging equipment in the biotechnology sector. The ideal candidate will have over 5 years of experience in validation or commissioning within pharmaceutical or biotech environments. You will be responsible for developing documentation and ensuring compliance with FDA and cGMP regulations, making this a critical role in maintaining high-quality standards. Join a dynamic team that values collaboration and innovation. #J-18808-Ljbffr