1 to 3 of 3 Permanent GMP Jobs in the West Midlands

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »

to help our patients. We value and encourage learning and development. As the Quality Assurance officer you will support the QA Manager in overseeing GMP compliance, contribute to the management of QMS and ensure the maintenance of quality certifications and standards throughout the manufacturing, testing and release of the product. … companies QMS. · Support with assessment of deviation event investigations. · Support closure to plan of Change Controls and CAPA actions. · Issue, review and approval of GMP batch manufacturing records to support certification and release. · Assist in performance of internal self-inspection audits. · Support the Company’s Quality Meetings. · Assist in maintaining … the Company’s quality certifications, e.g. GMP, GDP, HO approvals, etc. · Assist in preparation for inspections from MHRA and other Competent Authorities · Provide quality review and input to manufacturing and business activities. · Ensure compliance with the Company’s Quality Standards. · Engage with the wider team and sector to gain wider more »

cell therapies for established applications as well as first in man studies. Main duties of the job In this role you will be performing GMP production and interpreting novel recombinant proteins or Cell and Gene therapy clinical grade products manufactured on behalf of NHSBT for clinical trials. Operating a range … Post holders will work at the level of responsibility and to the standards of conduct and performance expected of a graduate Scientist. Following initial GMP production ensure any subsequent follow up investigations or actions are identified and initiated. Communicating complex information, including technical and scientific analysis, verbally, in writing and … electronically. Contributing to the GMP production service leading to release of reports or products. Assisting in training and supervision of support staff. You will be required to travel and spend time away from base, which will involve working irregular hours and overnight stays when required, with prior notice. You will more »