1 to 2 of 2 Permanent GMP Jobs in Devon

fixed weekly rotation. Responsibilities: Perform routine quality control examinations. Conduct routine analysis of raw materials and products using various techniques. Ensure all work is GMP compliant. Use a variety of instrumental and wet chemistry techniques to ensure analysis is accurate. Ensure consistent production of high-quality self-care products. Key more »

requirements of IT infrastructure transitions. Ensure that validation protocols adhere to regulatory standards, including FDA and MHRA guidelines, FDA 21 CFR Part 11, EU GMP Annex 11 and align with company policies and procedures. Develop and execute validation protocols and test scripts for IT systems and equipment to ensure compliance … experience in CSV, validation, or quality assurance role within the pharmaceutical industry. Proficiency in CSV principles, regulations (e.g., FDA 21 CFR Part 11, EU GMP Annex 11), and guidelines (e.g., GAMP 5). Strong understanding of IT systems, networks, and infrastructure components, including servers, databases, and software applications. Experience with more »