Back to Job SearchROLE OVERVIEW
We are currently looking for a Site Engineer to join a leading radiopharmaceutical production company based in a central location. This exciting opportunity is ideal for a technically skilled engineer with a passion for ensuring operational excellence and regulatory compliance in a highly regulated environment. The successful candidate will play a crucial role in maintaining and validating complex production equipment used for radiopharmaceutical manufacturing, supporting patient imaging and diagnostic services.
This dynamic role offers the chance to work within a cutting-edge sector, collaborating with multidisciplinary teams to deliver safe, reliable, and compliant production processes. The Site Engineer will be instrumental in maintaining high standards of quality, safety, and operational efficiency at our client’s site.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Site Engineer will be varied however the key duties and responsibilities are as follows:
• Oversee the functional operation, maintenance, and validation of production equipment related to the synthesis of 18F radiopharmaceuticals, ensuring compliance with GMP and regulatory standards.
• Arrange and carry out scheduled and emergency maintenance for critical plant equipment, including cyclotrons, synthesisers, dispensing systems, and hot cells.
• Lead validation activities for new processes and equipment, preparing documentation such as VMP, URS, IQ, OQ, PQ, and PV, and supporting validation lifecycle management.
• Provide engineering support to production teams, including training staff in equipment operation and maintenance, and liaising with external contractors and OEMs to ensure quick resolution of faults.
• As the Site Engineer, you will monitor faults, implement troubleshooting strategies, and collaborate with teams to ensure minimal downtime and continuous production.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Site Engineer we are looking to identify the following on your profile and past history:
• A Degree or higher level in Engineering or a relevant scientific/technical field (e.g., Biomedical Engineering, Mechanical/Electrical Engineering).
• Proven experience in maintenance, validation, and operation of complex production or laboratory equipment, ideally within a regulated GMP environment.
• Knowledge of radiation safety procedures, including site radiation protection practices and waste management protocols.
• Extensive experience working with high-precision machinery such as cyclotrons and synthesizers, with a focus on operational reliability and safety.
WHAT’S IN IT FOR YOU?
Joining our client offers you the opportunity to develop your career within a pioneering organisation dedicated to advancing medical imaging and diagnostics. You will benefit from working within a supportive, innovative environment and contribute to life-changing medical treatments. The role provides a platform for career progression in the highly specialised field of radiopharmaceutical production.
Key Words: engineering / maintenance / validation / GMP / radiopharmaceuticals / regulatory compliance / training / fault troubleshooting / equipment development / radiation safety
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
