GMP Validation Specialist - Biopharma (On Site, 12m)

A biopharmaceutical company is seeking a Validation Specialist at their Elstree facility on a 12-month fixed term contract. This role supports compliance and validation activities within a highly regulated environment. Candidates should possess a degree in a science or engineering discipline and significant experience in biopharmaceutical validation. The position requires attention to detail and a commitment to continuous improvement. The role is fully on-site, with a focus on ensuring product quality and patient safety.