Responsibilities Collaborate with system owners to design and maintain compliant, efficient quality systems supporting GMS and product lifecycle. Oversee data integrity and act as system administrator for key Quality Systems. Manage site Quality System Governance, ensuring compliance with company standards and regulatory requirements. Evaluate, approve, and monitor suppliers, including managing quality agreements. Lead change control processes and handle regulatory submissions. Support inspection readiness programs, including audits and regulatory inspections. Review and approve analytical method transfers, protocols, and related investigations. Manage GMP documentation, site validation plans, and the development of the site training system for GMP activities. Requirements Bachelor's degree in pharmaceutical, biological, or similar. 4+ years of 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 management GMP auditing systems