Quality Assurance Project Document Controller

Due to significant expansion, we have a fantastic opportunity for a Quality Assurance Project Document Controller to join our Radiopharmacy Quality Assurance team. If you have experience in Document Control within a GMP environment, an excellent grasp of Microsoft Office programs, top-class typing and report writing skills, a time-oriented approach to handling queries and tasks and detail-focused document organizing abilities, then this may be the opportunity you are looking for. The Document Controller will be an active member of the Quality Assurance Team, responsible for supporting the QA Manager in managing the QA Document Control System and tracking training compliance to ensure the site complies with quality objectives, company procedures and regulatory requirements. The QA department oversees GMP compliance and the effectiveness of the Quality Management Systems supporting the manufacturing, testing and release of the product. Prior experience within a radiopharmaceutical setting is desirable. Experience in Good Manufacturing Practice (GMP) is essential.