In this role, you will support the validation and qualification of GMP-critical equipment, facilities, and systems to ensure compliance with regulatory standards. You will collaborate with cross-functional teams to maintain validated states, review validation documents, and assess change controls. Your expertise will help uphold a high-quality, compliant manufacturing environment in the cell and gene therapy space.
Start Date: 01/09/2025
Duration: 12 Months
Place of Work: Visp