GMP CSV Specialist: IT & Automation Validation

A leading services supplier is seeking a Computerized Systems Validation (CSV) Specialist in Clayton, North Carolina. The role involves ensuring compliance and managing validation activities for IT/Automation systems in a biopharmaceutical environment. Candidates must have a Bachelor's degree in relevant fields and 3–7+ years of experience in CSV. Strong organization, communication skills, and hands-on experience with HP ALM are essential for success in this challenging position. Competitive salary and professional growth opportunities offered. #J-18808-Ljbffr