CQV Validation Specialist for Biotech Downstream Equipment

A leading services supplier in biotech is seeking a Validation Specialist for commissioning and qualification of downstream process equipment in a GMP-compliant facility. Candidates should hold a Bachelor’s degree and have 3-7 years of CQV experience in biotech or pharmaceutical environments. Responsibilities include executing protocols and ensuring compliance with regulatory standards. The ideal candidate will demonstrate strong communication, documentation skills and familiarity with electronic validation systems, including Valgenesis and Kneat. #J-18808-Ljbffr