To prepare cancer chemotherapy and medicines for injection manufactured under section 10 exemption of the Medicines Act 1968, using isolator technology, providing all necessary in-process checks, within the clean room environment under the guidance of good manufacturing practice.To prepare chemotherapy for intrathecal use according to Department of health guidelines, local trust policy and departmental procedures.To supervise, train and complete competency assessments of Assistant Technical Officers, rotational technicians and student technicians in the preparation of specified products including, medicines for injection and cancer chemotherapy under the guidance of the senior specialist technicians.To follow carefully all standard operating procedures to ensure all products are made safely and efficiently in accordance with Good Manufacturing Practice guidelines.To prepare all types of product documentation, including electronic worksheets with all types of calculations, and the production of labels using the Prisym 2000 label software. To supervise the documentation room, answering simple queries from ward staff and influencing the flow of work into the preparation area. To participate in the preparation of clinical trials completing all necessary documentation as described in the study protocol. To assemble the raw materials and consumables required to prepare each individual product, ensuring total segregation of each preparation using a box or tray segregation system as defined in the standard operating procedure. To prepare master product documentation under the supervision of the senior specialist technicians. To partner the specialist senior technician or production team manager in the recruitment and selection process for Assistant Technical Officers. To conduct an individual performance review in liaison with the production team manager for each Assistant Technical Officer to ensure continued professional development. To complete any environmental monitoring or operator validation tests requested by the quality assurance manager. To assist with stock control to include the production and checking of routine stock checks, ensuring stock rotation and expiry date checks are completed and investigating stock discrepancies. To complete, maintain and file all relevant documents, records and reports. To clean the pharmacy aseptic suite and support rooms following standard operating procedures and using specific methods of cleaning, ensuring appropriate quality control samples are taken and cleaning logs filled out. To cover the delivery and collection of items to the wards and other departments in the absence of Aseptic services ATOs. To cover the transfer of waste for disposal, some of which is hazardous from the pharmacy to the collection point in the absence of technical services ATOs. To co-operate and participate in any training and development in Aseptic services, attending such study days and courses as necessary for service development.