5 Permanent GMP Jobs in the East Midlands

team. Ensure all Radio pharmacy work complies with statutory regulations and good practice codes; the latter including. The EU Guidance on Good Manufacturing Practice (GMP)/Rules and Guidance for Pharmaceutical Manufacturers and Distributors published by the MHRA. Define, in conjunction with the Head of Nuclear Medicine, Radio pharmacy production … relevant business cases, financial planning and clinical governance where new service developments are proposed. Together with the Head of Nuclear Medicine and the trusts GMP Quality controller act as the Trust expert for the safe use and introduction of all radiopharmaceuticals. Manage specialist staff rotas/leave arrangement to ensure … good scientific knowledge (degree level). An in depth knowledge of the theory and practice of radiopharmaceutical production Detailed knowledge of Good Manufacturing Practice (GMP) An in depth knowledge of the practices and procedures associated with the use of radiopharmaceuticals for routine nuclear medicine investigations A good knowledge of the more »

satisfy the requirements of external agencies. Responsible for timely and accurate reporting of internal Refresco KPIs to the management team. Be responsible for ensuring GMP and Hygiene standards are communicated to the operational teams and processes are in place to effectively monitor and manage them. Partake in site visits and more »

maintained and up to date. Education and experience : *Degree in chemistry, analytical chemistry or equivalent *Previous experience of HPLC, GC analysis with pharmaceutical/GMP regulated environment *Previous experience in analytical method transfer, cleaning validation *your previous experience could be QC analyst, stability analyst, development analyst, principal analyst and raw more »

on a WDA license as a Responsible Person or Responsible Person Import (RPi) Significant experience leading and developing a team GMP | GDP | GMDP | Good Manufacturing Practice | Good Distribution Practice | WDA | RP | Responsible Person | Head of Quality | Quality Director | Quality Manager | Wholesale Distribution License more »

pharmaceutical environment/Medical Device industry required Technical experience within the Manufacturing functions of a pharmaceutical company. Technical knowledge of Pharmaceutical Packaging. Vendor Audits (GMP, Technical and EHS) Knowledge in Supply Chain Risk management, GMP, Quality System requirements, the ‘Orange Guide’, equivalent FDA regulations and systems, procedures, products and organisation. more »