CQV Validation Specialist for Biotech Downstream Equipment

A leading services supplier is seeking a Verification Specialist to support the commissioning and qualification of downstream process equipment in a GMP-compliant facility. Responsibilities include developing and executing protocols, coordinating with vendors, and ensuring compliance with regulatory standards. The ideal candidate has 3–7 years of CQV experience and a bachelor’s degree in a relevant field. This role offers an opportunity to work in a dynamic environment within the biotech industry. #J-18808-Ljbffr