Actively participate in meetings and work programmes to assess and investigate safety signals involving sterilisation; effective management of safety issues ensuring relevant assessors are kept up-to-date and quality of work is maintained. You will provide specialist technical advice and support on sterilisation to other colleagues and senior officials to meet divisional business needs and targets. As well as undertake technical reviews of sterilisation issues as required on new and emerging safety signals and/or new and emerging data/evidence and make recommendations for actions to protect patients. The successful candidate will have a degree or equivalent qualification in life sciences, health care or engineering (such as medical engineering, toxicology, material science, or healthcare qualification); and previous relevant experience gained in healthcare, medical device manufacturing, regulatory environment, or health data science. Our successful candidate will have: Knowledge or practical experience of medical devices Experience of critically analysing complex clinical/scientific/technical information from a number of sources under pressure and make appropriate recommendations or decisions to protect patient safety/public health even when the evidence is not clear. Implement appropriate actions to mitigate risk Evidence of writing well-structured, concise, reports to support decision making and provide information to stakeholders. Awareness of the regulatory frameworks Closing date: 12 April 2026

Actively participate in meetings and work programmes to assess and investigate safety signals involving sterilisation; effective management of safety issues ensuring relevant assessors are kept up-to-date and quality of work is maintained. You will provide specialist technical advice and support on sterilisation to other colleagues and senior officials to meet divisional business needs and targets. As well as undertake technical reviews of sterilisation issues as required on new and emerging safety signals and/or new and emerging data/evidence and make recommendations for actions to protect patients. The successful candidate will have a degree or equivalent qualification in life sciences, health care or engineering (such as medical engineering, toxicology, material science, or healthcare qualification); and previous relevant experience gained in healthcare, medical device manufacturing, regulatory environment, or health data science. Our successful candidate will have: Knowledge or practical experience of medical devices Experience of critically analysing complex clinical/scientific/technical information from a number of sources under pressure and make appropriate recommendations or decisions to protect patient safety/public health even when the evidence is not clear. Implement appropriate actions to mitigate risk Evidence of writing well-structured, concise, reports to support decision making and provide information to stakeholders. Awareness of the regulatory frameworks Closing date: 12 April 2026