CQV Specialist: Packaging Systems for Biotech & Pharma

A leading validation and engineering company is seeking a CQV Specialist to support commissioning, qualification, and validation activities in biotechnology manufacturing. The ideal candidate will have a Bachelor's degree in Engineering or Life Sciences, and at least 5 years of experience in CQV within a regulated environment. This role includes developing validation documentation and coordinating with cross-functional teams to ensure compliance with industry regulations. A commitment to high ethical standards is essential, alongside strong technical writing skills. #J-18808-Ljbffr