Validation & CSV Specialist (GxP IT)

A global pharmaceutical company in Pennsylvania seeks a Validation Specialist responsible for managing GxP Application Inventory and supporting Computer System Validation (CSV) documentation. The role involves ensuring compliance with regulatory requirements, vendor coordination, and conducting validation activities with a focus on continuous improvement. Candidates should have 7-8 years of IT experience in pharma manufacturing and must hold relevant educational qualifications. Join a dynamic environment that prioritizes professional growth. #J-18808-Ljbffr