Lead Specialist in Radiopharmacy

6 months ago

Brighton, United Kingdom 279 University Hospitals Sussex NHS Foundation Trust Full time

This is an exciting opportunity to join the Radiopharmacy team at the Royal Sussex County Hospital in Brighton. The licensed unit supplies radiopharmaceuticals to three Nuclear Medicine departments in local hospitals. We will shortly be moving to a purpose-built department in a brand new, modern and innovative hospital and are looking to expand the service and the workforce. We are seeking an enthusiastic and motivated professional team player with previous experience of manufacturing radiopharmaceuticals and exceptional organisation and communication skills. The impending move into the new hospital will provide an opportunity for expansion of the current Radiopharmacy service in both scale and scope and would suit a dynamic individual who is looking to broaden their experience and to make a positive contribution to the future development of the UHSussex Radiopharmacy.

We are looking for someone to take a leading role in the Quality Assurance for the department. The role also includes supporting the delivery of a comprehensive, efficient and high quality clinical Radiopharmacy service to the Trust and external customers. The key aspects include participation in the manufacture and quality control testing of radiopharmaceuticals and supporting the effective operation of the Quality Management System developed and maintained by the Radiopharmacy covering documentation management, recording and investigation of non-conformances and deviations and the change control process.

The successful applicant will be expected to act as a Radiation Protection Supervisor, so should have good knowledge of relevant legislation related to working with radioactive materials (including IRR and IR(ME)R ), although training will be provided if necessary.

The post involves line management responsibility for a Band 3 Radiopharmacy Technician and will include the training of other staff / students.

Staff are required to have a flexible approach to working hours. The normal hours of the department are from 04:30 - 15:00 and staff work different shifts to cover the service provision, with start times varying between 04:30 - 07:00 on a rotational basis. There may also be occasions when duties may sometimes have to be performed outside of the normal working hours of the Department e.g., at weekends.

About our Trust

At UHSussex we’re proud to be at the heart of the NHS. As one of the UK’s largest acute Trusts, we’re a leading example of the excellence, the ambition and the values that have embodied the NHS for over 70 years.

**Improving lives**:
We are a vibrant and inclusive organisation, with patient care at our core.

We treat our patients and staff with the same compassion and empathy we expect for ourselves. We’re here for them when they need us, and we go above and beyond to meet their needs.

**Build a career with us**:
As a university trust and a leader in healthcare research, we value learning, teaching and training so that we can be the best that we can be. From the moment you start with us, and throughout your career, we will help you to grow and develop. We hope that in choosing UHSussex, you are choosing a long and happy career where you will be able to see the difference you make and feel valued for all that you do. In return for your commitment to us, we will provide on-going support for your professional development, as well as a friendly, challenging and stimulating work environment.

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 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 assist in the qualification of the new state of the art

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