GMP CSV Specialist: IT & Automation Validation

A leading technology solutions firm in Clayton, North Carolina is seeking a Computerized Systems Validation Specialist to support system upgrades and validation in a biopharmaceutical environment. The ideal candidate will have 3–7 years of CSV experience aligned with regulatory standards such as 21 CFR Part 11. Responsibilities include developing validation documentation, executing qualification testing in HP ALM, and collaborating with cross-functional teams to ensure compliance. Competitive compensation and growth opportunities offered. #J-18808-Ljbffr