Medicines and Healthcare products Regulatory Agency
Policy Advisor - £37,456 - £42,084 p.a. + benefits
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Job Summary
We are currently looking for a Policy Advisor to join our Legislative Delivery Team within the Strategy group.
This is a full-time opportunity, on a permanent basis. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU.
Government departments and agencies are working towards implementing a minimum 60% attendance in office sites.
We are currently implementing a flexible, hybrid way of working, with a minimum of 8 days per month working on site to enable the collaboration and contact with partners and stakeholders needed to deliver MHRA business. Attendance on site is driven by business needs so depending on the nature of the role, this can flex up to 12 days a month, with the remainder of time worked either remotely or in the office. Some roles will need to be on site more regularly. Remote working is potentially available for some specific roles. Please discuss this with the recruiting manager before accepting an appointment.
Who are we?
The Medicines and Healthcare products Regulatory Agency enhance and improve the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research.
The Strategy Group is a new group within the Agency that brings together policy, regulatory reform, legislative delivery, strategic coordination and stakeholder-engagement functions, helping to develop and coordinate cross-cutting work that supports MHRA corporate priorities. The broader group focuses on issues that are at the heart of public health – fast, safe access to medicines and medical devices, working with industry and NHS and other health Arms-length bodies (ALBs); and supporting the future of the life sciences industry in the UK. We do all this while ensuring patients are at the heart of our work.
Policy and Regulatory Reform is a division of the Strategy Group. We are made up of three small, closely connected teams, Regulatory Strategy, Policy, and Legislation Delivery. Together we have central oversight of the Agency’s regulatory reform agenda, and we seek to strengthen the regulatory environment in a way that safeguards public health and supports access to safe, innovative and effective healthcare. The work of the Legislation Delivery team supports the MHRA to navigate policy and legislative processes with confidence and clarity and enables consistent, high-quality decision-making and delivery.
Job Description
The Legislative Delivery team are the Agency’s experts in delivering primary legislation and specific statutory instruments across medicines, medical devices and fees. You will play a vital role in progressing the Agency’s priorities, working with experts across the agency to develop and implement legislation on high profile issues which have a tangible impact on public health, patients, and the life sciences industry. Working closely with subject matter experts and technical teams, the team anticipate requirements and guide projects efficiently through each stage of the legislative process. They also work closely with colleagues across government to anticipate and respond to wider changes which will impact the Agency’s regulatory framework, and to identify opportunities to take forward legislative changes as part of a prioritisation process.
We are currently working on a range of primary and secondary legislative reforms, as well as contributing to designing the future legislative pipeline for the Agency.
The role will present great opportunities to collaborate with experts across the MHRA, DHSC, other Government departments, and external health organisations. You will work collaboratively with different functional teams to bring in different perspectives and develop a strong understanding of the regulatory landscape and healthcare environment.
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Key Responsibilities:
- Support legislative initiatives: Manage elements of the MHRA’s legislation work for medicines and medical devices. Work closely with technical colleagues across the Agency, DHSC and lawyers to develop and refine new legislative proposals and to triage and prioritise legislation requests.
- Enabling Regulatory Development: Convene groups of technical experts, providing secretariat support, bringing colleagues from across the agency together to solve arising issues or develop new regulatory approaches.
- Stakeholder Engagement: Prepare consultations and understand stakeholder views to inform proposals for regulatory reform to ensure they will deliver for stakeholders including patients, life sciences industry and research community.
- Policy Development: Communicate complex regulatory policy and draft concise recommendations, advice and briefings on regulatory reform proposals, to support senior leaders and Ministers in key decision making.
- Coordination of Regulatory Reform Responses: Support the Agency’s responses to requests on regulatory reform from other government departments or external stakeholders, coordinating across the Agency and keeping track to ensure responses are delivered in a timely manner.
- Legislation Management: Support new legislation through cross-government clearances and parliamentary process, setting out project plans and ensuring the process progresses to agreed timelines.
- Project Management: Coordinate the delivery of legislative projects across multidisciplinary teams, establishing clear plans and responsibilities, monitoring progress and risks, and keeping stakeholders informed throughout the project lifecycle.
Person specification
Essential Criteria:
- Experience in a relevant area in the civil service or other organisations, which give understanding of working in or with the public sector.
- Previous experience working in health, life sciences or regulation environment. (Desirable)
- Previous experience working on legislation. (Desirable)
Behaviours
We'll assess you against these behaviours during the selection process:
- Working Together
- Delivering at Pace
- Communicating and Influencing
- Making Effective Decisions
Benefits
Alongside your salary of £37,456, Medicines and Healthcare Products Regulatory Agency contributes £10,851 towards you being a member of the Civil Service Defined Benefit Pension scheme. Find out what benefits a Civil Service Pension provides (opens in a new window).
- Annual Leave: 25 days annual leave on entry, rising by one day for each completed year of service to a maximum of 30 days and pro-rata for part-time staff. PLUS 8 bank holidays
- Privilege Leave: 1 day
- Hours of Work: 37 hours (net) per week for full time staff in all geographical locations, including London and pro rata for part-time staff
- Occupational Sick Pay (OSP): One month full pay/one month half pay on entry, rising by one month for each completed year of service to a maximum of six months full pay and six months half pay after five years’ service.
- Mobility: Mobility clause in contracts allowing staff to be mobile across the Civil Service
- Civil Service Pension Scheme: Please see the link for further information http://www.civilservicepensionscheme.org.uk. For enquiries relating to the Civil Service Pension Schemes please contact MyCSP's Pension Service Centre directly on 0300 123 6666
- Flexible working: to ensure staff maintain a healthy work-life balance
- Interest free season ticket loan or bike loan
- Employee Assistance Services: and access to the Civil Service Benevolent Fund
- Eligibility to join Motoring, Boundless by CSMA
- Variety of staff and Civil Service clubs
- On-going learning and development
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Artificial intelligence
Artificial intelligence can be a useful tool to support your application, however, all examples and statements provided must be truthful, factually accurate and taken directly from your own experience. Where plagiarism has been identified (presenting the ideas and experiences of others, or generated by artificial intelligence, as your own) applications may be withdrawn and internal candidates may be subject to disciplinary action. Please see our candidate guidance (opens in a new window) for more information on appropriate and inappropriate use.
Selection process details
This vacancy is using Success Profiles (opens in a new window), and will assess your Behaviours, Strengths and Experience.
The Selection Process:
- We use the Civil Service Success Profiles to assess our candidates, find out more here.
- Online application form, including questions based on the Behaviour, Experience and Technical Success Profiles. Please ensure all application questions are completed in full; your application may not be considered if any responses are left blank.
- Interview, which can include questions based on the Behaviour, Experience, Technical and Strengths Success Profiles.
- An anonymised CV outlining your job history and previous skills/experience that demonstrate how you meet the essential criteria.
In the instance that we receive a high number of applications, we will hold an initial sift based on the lead criteria of: Working Together
Applicants are assessed on whether they meet any mandatory requirements as well as the necessary skills and experience for the role. Applications are scored based on the competency-based answers provided- ensure you have read these thoroughly and allow sufficient time. You can view the competencies for this role in the job description.
If you require any disability related adjustments at any point during the process, please contact careers@mhra.gov.uk as soon as possible.
Important Dates:
- Closing date: 5th October 2026
- Shortlisting date: from 12th October 2026
- Interview date: from 26th October 2026
If you need assistance applying for this role or have any other questions, please contact careers@mhra.gov.uk
Additional Information
Candidates will be subject to UK immigration requirements as well as Civil Service nationality rules. Further information on whether you are able to apply is available here.
Successful candidates must pass a disclosure and barring security check as well as animal rights and pro-life activism checks. People working with government assets must complete basic personnel security standard checks.
Certain Roles Within The MHRA Will Require Post Holders To Have Vaccinations, And In Some Circumstances, Routine Health Surveillance. These Roles Include:
- Laboratory-based roles working directly with known pathogens
- Maintenance roles, particularly those
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