3 of 3 GMP Jobs in the North East

and process transfer expected to exceed 5 years. Prior experience with biopharmaceutical product registration preferably with FDA and/or EMEA. Knowledge of current GMP's, ICH Guidelines, and FDA/EU validation practices for biopharmaceutical processes required. Preferred Qualifications: If you have the following characteristics, it would be a More ❯

continuous improvement initiatives, manage minor projects ( In this role, you will Work collaboratively to improve equipment performance and reliability. Follow SOPs/SWs, ensure GMP compliance, report quality issues, and uphold safety standards. Maintain all training requirements via the 'My Learning' platform. Participate in Continuous Improvement activities, including DMAIC, RCA More ❯

experience of automation delivery on multiple projects in the pharmaceutical industry. Knowledge of industry standards and systems is essential, alongside a good understanding of GMP requirements for automated systems. The role requires delivery of results on time, in accordance with client standards and health and safety procedures. The successful candidate More ❯