Diagnostic Regulatory Specialist – Innovative Devices, Health Quality and Access Group
This is a full‑time, fixed‑term role (until 31 March 2029) based at 10 South Colonnade, Canary Wharf, London.
Key responsibilities
- Take ownership of delivering key elements of the new medical devices regulatory regime, including contributing scientific, technical and policy input to future legislation and implementation.
- Provide scientific, technical and policy input to support implementation of the regulatory framework through clear guidance and regulatory advice.
- Oversee delivery of the in vitro Diagnostics (IVD) roadmap, tracking progress against milestones and coordinating input across teams.
- Support international engagement with other regulators, including at the International Medical Devices Regulators Forum (IMDRF).
Qualifications
- Minimum of a Bachelor’s degree or equivalent experience.
- Working knowledge of UK and/or EU medical devices legislation.
- Experience communicating with a range of stakeholders in the development and/or delivery of policy objectives.
- Experience with policy development in a regulatory environment, with ability to draft a range of policy and guidance documents for different audiences.
Diagnostic Regulatory Specialist employer: Medicines and Healthcare Products Regulatory Agency
The Medicines and Healthcare products Regulatory Agency (MHRA) is an exceptional employer, offering a dynamic work environment in the heart of Canary Wharf, London. With a strong commitment to employee growth, the agency provides opportunities for professional development and collaboration with leading experts in healthcare and research. The hybrid working model promotes a healthy work-life balance, while the agency's focus on innovation and public health ensures that employees contribute to meaningful projects that enhance the well-being of millions.
Contact Details:
Medicines and Healthcare Products Regulatory Agency Recruitment Team
