4 of 4 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 ❯

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 ❯

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 ❯

facility in North East England. This role offers the opportunity to be part of a high-performing automation team delivering critical systems in a GMP-regulated environment. Responsibilities: Executing FAT/SAT/IOQ protocols including generation of protocols and reports. Design, configure, and support Emerson DeltaV PCS and/… systems in collaboration with CQV and Operations teams. Participate in the development, testing, and deployment of automation changes, and maintain documentation in compliance with GMP requirements. Provide technical input during design reviews, FATs, SATs, and system walkdowns. Qualifications & Experience: Bachelor’s degree in Automation Engineering, Software Engineering, or a related … programming, troubleshooting, and control system configuration. Excellent communication and collaboration skills; comfortable working within a cross-functional, site-based automation team. Strong understanding of GMP, validation, and change control processes. More ❯