Specialist in GMP Documentation and Quality Assurance in Quality Management

Join Brunel and advance your career by working with renowned clients across various industries. As a Specialist in GMP Documentation and Quality Assurance, you will handle batch documentation, create and maintain GMP documents, track deviations, support release documentation, and manage data and document archiving. Candidates with a background in pharmaceutical, scientific, technical, or commercial fields are welcome, including recent graduates and those with some experience in pharma or GMP environments.