Regulatory Affairs Lead
The Regulatory Affairs Lead provides essential support to the Medicines and Healthcare Products Regulatory Agency's proactive market surveillance and approved body teams by planning audits, reviewing technical documentation, and managing device registrations. Working closely with senior management, regulatory specialists, and external stakeholders, the post holder helps ensure compliance with medical device regulations and drives key projects. This role plays a vital part in identifying market trends, assessing risks, and shaping the agency's regulatory approach to medical devices.
What they're looking for
- Knowledge of Medical Device Regulations and regulatory reporting
- Ability to assess the impact of policy and regulatory changes
- Experience coordinating or delivering projects to deadlines
- Proven initiative in proposing solutions and driving improvements
Qualifications
- University degree or equivalent knowledge and experience
Nationality requirements
Open to UK, Irish, Commonwealth, EU, and Turkish nationals with relevant right to work or EUSS status.
Selection process
Shortlisting from 06 October 2026. Interviews take place from w/c 19 October 2026 and include a presentation and interview.
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