Aseptic / Clinical Trials Pharmacist

You will be able to find a full Job description and Person Specification attached within the supporting documents or please click Apply now to view in Trac. Why SMPU? Be part of a specialist NHS unit with a reputation for excellence. Work on ground breaking clinical trials shaping future care. Gain exposure to licensed production & expand regulatory knowledge. Enjoy professional development, flexible working & NHS benefits. Apply now & help deliver life-changing therapies while supporting vital research. To plan, implement, maintain and evaluate clinical production activities including staff, resources, activity, processes, and information, ensuring the highest level of professional standards of service are provided, encompassing both quality and timeliness of service to patients. To manage the overall workload in accordance with the capacity plan ensuring staff rotas reflect an appropriate skill mix for the allocated tasks and are an effective use of staff time, prioritising and adjusting plans as required. To be responsible for ensuring all equipment is validated and functioning correctly, and all plant and equipment planned preventative and corrective maintenance is carried out. To manage the environmental monitoring processes in line with current guidance and to ensure correct action is taken in the event of a deviation. This will include liaising with the Quality Assurance team where appropriate to resolve any validation or monitoring issues. To develop distribution systems and processes under controlled conditions. To ensure that all staff adhere to hygiene and clothing policies associated with their work within the controlled cleanroom environment. This involves strict hand washing procedures andchanging into designated cleanroom clothing. To ensure the digital systems are fit for purpose and approve accuracy of master process and procedure documentation. To contribute to the update and maintenance of the Site Master File in collaboration with the Production Manager and Quality Assurance Lead, analysing data from several sources andpresenting findings for internal use and publication, when required. To be responsible for the handling of Controlled drugs in accordance with professional, ethical and legal guidelines.