Radiopharmacy Technician

The post holder will be involved from the early stages of the project which will involve drafting documentation including SOPs and validation protocols for review. Executing validation protocols for the production and quality control of radiopharmaceutical products. Upon completion of the project the post holder will participate in the GMP production, sterile and aseptic dispensing, and quality control of PET radiotracers for clinical use.

Operating a range of automated and manual radio chemical synthesis and quality control equipment. The role also involves assisting in all aspects of operating and maintain the facility to GMP standards, including documentation, equipment and laboratory maintenance including cleaning, environmental monitoring, incoming materials management, and stock control.

The position is located at Newcastle.

The post holder will be involved from the early stages of the project which will involve drafting documentation including SOPs and validation protocols for review. Executing validation protocols for the production and quality control of radiopharmaceutical products. Upon completion of the project the post holder will participate in the GMP production, sterile and aseptic dispensing, and quality control of PET radiotracers for clinical use.

Operating a range of automated and manual radio chemical synthesis and quality control equipment. The role also involves assisting in all aspects of operating and maintain the facility to GMP standards, including documentation, equipment and laboratory maintenance including cleaning, environmental monitoring, incoming materials management, and stock control.

• Manufacture PET radiopharmaceuticals using hot cell and isolators;
• Sanitisation/cleaning aseptic suite facilities;
• Aseptic dispensing of PET radiopharmaceuticals using negative pressure isolator technology;
• Adopting radiation protection technique at all times ALARA;
• Packing and dispatch of radiopharmaceuticals according to local guidelines and transport regulations;
• Collating received orders and inputting them into the dispensing database;
• To carry out staff training and knowledge sharing when applicable;
• Sanitation and transferring of consumables in the aseptic suite and isolators;
• Cleaning the isolators and Radiopharmacy facility according to SOP’s;
• Aseptic Suite monitoring including Environmental monitoring, Radiations monitoring;
• First line maintenance of equipment;
• Carry out Quality Control procedures analysing the radionuclide and radio chemical purity of radiopharmaceuticals using standard analysis packages as specified in the European Pharmacopoeia;
• Undertake laboratory cleaning, maintenance and procedures required for GMP analysis of radiopharmaceuticals;
• Recording of the logs for fridge, freezers, isolator checks and all other logs;
• Raising and completing deviation reports where applicable;
• Participate in Root Cause Analysis and CAPA identification;
• Effective communication with all colleagues to facilitate efficiency in both production and quality related matters;
• Maintain paper and electronic records from all production processes for statutory purposes, including production and quality control under GMP;
• Assist in qualification/requalification exercise as required including preparing documentation and execution of protocols;
• Setting up production orders in the system, Checking stock level and ordering products;
• Adherence to legal and organizational procedures & guidelines about quality, safety, health and environmental issues;
• Comply with the requirements of the Pharmaceutical Good Manufacturing Practice (GMP), Ionising Radiation Local Rules, COSSH and Health & Safety procedure;
• Training of Technicians in PET manufacturing and QC processes, and standard operating procedures across the site.

• Degree in a scientific discipline (e.g., Chemistry, Pharmaceutical Sciences, Biology, Biomedical Science, Radiochemistry, or a related field);
• Knowledge of working within a GMP environment;
• Willingness to work flexibly on a rotating 12 hour shift pattern between 00:00 (midnight) to 17:00;
• Knowledge of Ionising Radiation Local Rules, COSSH and Health & Safety procedure (Desirable);
• Validation experience (Desirable);
• Aseptic dispensing or Radiopharmacy experience (Desirable);
• Working knowledge of pharmaceutical chemistry and good manufacturing practice is required;
• Ability to work independently and use own initiative;
• Strong communication and interpersonal skills;
• Excellent…