Onsite CSV Engineer: GMP Systems Validation & Compliance

An established industry player is seeking a Computer Validation Specialist to lead validation activities for GxP electronic systems. This role involves working cross-functionally to ensure compliance with health authority regulations while managing validation deliverables for critical systems. The ideal candidate will have a strong background in validation within the biotechnology or pharmaceutical sectors, demonstrating expertise in documentation and system integration. Join a dynamic team where your contributions will directly impact the quality and efficiency of drug product manufacturing, and be part of a collaborative environment that values your skills and insights. #J-18808-Ljbffr