Responsibilities Manage the key Quality Systems for the site (Veeva Vault, LMS). Oversee preparation, approval, and training upload of site documentation (GMP, EHS, operational procedures) in Veeva Vault and LMS. Track site documentation schedule, escalate issues, and support timely resolution. Administer LMS and ensure training documentation is accessible. Coordinate records retention and manage control of all records through the Records Management process/tools. Issue analytical records and logbooks for testing support. Provide document management metrics and training reports as needed. Requirements At least 2 years of experience in a similar position Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003 Skills: documentation quality GMP pharmaceuticals