4 Permanent GMP Jobs in Bristol

with you. Main duties of the job To assemble and prepare pharmaceutical products in accordance with relevant Standard Operating ProceduresPrepare, in accordance with Good Manufacturing Practice, Aseptic injectables using isolator technologyTo accurately record and maintain all elements of paper-work related to the preparation of products and maintenance of the … Services and support the delivery of their trainingTo assist in the maintenance of the environment, ensuring that the cleanliness of the facility is to GMP standards About us North Bristol NHS Trust employs over 12,000 staff providing healthcare to the residents of Bristol, South Gloucestershire and North Somerset from … procedures Undertakes the physical and microbiological environmental monitoring associated with the facility. Undertakes the regular daily cleaning of the aseptic facility in accordance with GMP and departmental procedures Undertake the monthly and 3 monthly deep clean processes. Assemble non-sterile packs of emergency medication in line with departmental procedures and more »

Pharmacy or Pharmacy Technical Services, particularly chemotherapy; or clinical pharmacy experience across a range of specialised areas (Band 7) Knowledge of Good Manufacturing Practice (GMP) and professional standards (Band 7) Desirable Working knowledge of systemic anti-cancer treatments and supportive care Post-registration experience in Cancer Pharmacy, or Pharmacy Technical … Services particularly SACT; or clinical pharmacy experience across a range of specialised areas (Band 6) Knowledge of Good Manufacturing Practice (GMP) and professional standards (Band 6) Skills and abilities Essential Good oral and written communication skills, including the ability to communicate complex information Methodical and accurate Ability to assess priorities 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 »

out by all departments. ·Conduct shelf-life trials and record results accurately. ·To ensure equipment is calibrated and checked as per schedule. ·To complete GMP, glass and internal audits as required. ·To work closely with the intake team on raw material, packaging and label receipt and ensure any non-conformances more »