Candidate Information Pack: Please see JD for full details The post-holder will be required to comply with relevant statutory requirements relating to the manufacture of radioactive medicinal products, including those related to Good Manufacturing Practice as defined in The Rules and Guidance for Pharmaceutical Manufacturers and Distributors (Medicines and Healthcare products Regulatory Agency). The post-holder will participate in the rota for the manufacturing and take a leading role in the quality control testing programme for diagnostic and therapeutic radiopharmaceutical products for clinical use. In that capacity the post-holder will be required to act as a Radiopharmacy Operator, as defined by the Ionising Radiations (Medical Exposure) Regulations, 2017. The post-holder will be expected to act as an authorised releasing officer for products manufactured by the Radiopharmacy, performing, under delegated authority, the release of such products for clinical use. The post-holder will be required to consign radioactive materials to external sites, in compliance with the statutory requirements applying to the transportation of radioactive materials by road. The post-holder will participate in the effective operation of the Quality Management System operated by the Radiopharmacy. This will include management of documentation, recording and investigation of non-conformances and deviations and use of the change control process. The post-holder will be expected to contribute to the routine operation and maintenance of the Radiopharmacy facilities, including undertaking physical and microbiological environmental monitoring and cleaning of the facilities and equipment. The post-holder will take a leading role in qualification and validation of the facility and equipment. This will include managing the Asset Register and Permit to Work systems and ensuring that all equipment is maintained, calibrated and suitable for use.