1 to 3 of 3 GMP Jobs in Bristol

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

factory. * Monitoring customers returns and give daily the report to finance team. * To ensure that all operatives and staff within the factory comply with GMP and hygiene procedures and to advise and give training when this is not the case. * To work effectively within the departmental rota, ensuring all aspects … company procedures and policies. * To monitoring, verify and report any issues daily on Day & Night Shifts check list Compliance Audit. * To carry out Internal GMP/Glass and Hard Plastic Audit within the factory. * Weekly monitoring of all PPE request orders. * To ensure that all operatives and staff within the … factory comply with GMP and hygiene procedures and to advise when this is not the case. * To actively partake in the resolution of quality related issues. * To support training all members of staff in food hygiene, health & safety, manual handling, fire safety, chemical safety, and allergen awareness training. * To assist more »

with our long standing client in Bristol at an exciting time in their business where they will be commissioning a new Good Manufacturing Practice (GMP) facility. This will be in a new building and be a blank canvas for the new Quality Assurance and Validation Engineer to work on! You … will be working with colleagues both internal and external on commissioning and qualification of this new GMP facility. This will include equipment IQ/OQ/PQ activities, as well as validation and qualification of the ISO 7 and ISO 8 cleanrooms. You will be responsible broadly for all systems … self motivated with a can-do approach. Your background: Bachelors Degree in science or engineering with experience in facilities and equipment validation. Experience of GMP manufacturing, facilities, equipment qualifications and process validations, including cleanrooms. Knowledge of cGMP manufacturing regulations for the MHRA, FDA and other countries as required. Experience in more »