Lead Validation Specialist – GMP CSV

Job Description

A cell and gene therapy company in Scotland is seeking a Validation Supervisor to supervise a team involved in Computer System Validation (CSV). The role includes overseeing quality documentation, monitoring project milestones, and providing expertise during audits. Applicants should have a degree in Life Sciences or Computer Science and experience in a GMP environment. This is an exciting opportunity to make a significant impact in a rapidly expanding company.