A leading Biopharma client in the UK seeks a Process Validation Specialist for a 12-month contract. The role encompasses leading process validation activities in cell and gene therapy manufacturing. Candidates should have a proven track record in process validation and regulatory compliance, with hands-on experience in authoring necessary documentation. This is an excellent opportunity to contribute to cutting-edge projects while establishing yourself as a vital team member in a dynamic environment.#J-18808-Ljbffr…
