GMP CSV Specialist: IT & Automation Validation

A leading services supplier is looking for a Computerized Systems Validation (CSV) Specialist to support IT/Automation System upgrades in a regulated biopharmaceutical environment. The role involves ensuring compliance with industry regulations and executing validation activities. The ideal candidate holds a Bachelor's degree and has 3-7 years of experience in CSV, particularly with HP ALM. Strong organizational skills and attention to detail are essential for this position, which requires collaboration with various teams to develop and maintain validation documentation. #J-18808-Ljbffr