Responsibilities Ensure training documentation is current and accessible; support overall LMS functionality. Coordinate issuance and reconciliation of documents and labels to meet production and project timelines. Author and review technical documents, including SOPs, protocols, and reports. Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls. Collaborate across departments, external vendors, and global teams to meet documentation and compliance needs. Monitor documentation systems to ensure timely completion of Quality Management System tasks. Lead or support continuous improvement initiatives and operational technology improvements. Represent the QA team during internal audits and regulatory inspections. Identify and implement process improvements. Requirements Bachelor's degree in pharmaceutical, biological, or similar. 3+ years experience in the pharmaceutical industry 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: quality GMP pharmaceutical documentation