Cencora is seeking a Computer System Validation (CSV) Specialist to lead validation activities for GxP-critical systems, ensuring compliance with PIC/S Annex 11 and 21 CFR Part 11. The role interfaces with IT, QA, and external partners to deliver validated software and documentation. The ideal candidate has 3+ years' hands-on CSV validation experience in pharma/biotech, with a degree in CS/IT/engineering and robust communication and project-management skills.