IVD and Medical Devices Advisor in London

IVD and Medical Devices Advisor in London

London Full-Time 50000 - 60000 £ / year (est.) Home office (partial)
Medicines and Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Support the development of a new regulatory framework for medical devices and ensure quality service delivery.
  • Company: Join the Medicines and Healthcare products Regulatory Agency, enhancing health through innovation.
  • Benefits: Flexible hybrid working, competitive salary, and opportunities for professional growth.
  • Other info: Dynamic role with excellent career progression in a supportive environment.
  • Why this job: Be part of a transformative sector, shaping the future of medical device regulation.
  • Qualifications: Degree in relevant field and strong communication skills required.

The predicted salary is between 50000 - 60000 £ per year.

This vacancy is open to all Civil Service employees and employees of accredited non-departmental public bodies (NDPBs) who were appointed on merit following a fair and open competition; or were appointed to a permanent post through an exception in the Civil Service Commissioners' rules.

We are currently looking for an IVD and Medical Devices Advisor to join our Innovative Devices function within the Innovation and Compliance 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.

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 Innovation and Compliance (I&C) group delivers public health impact, world-leading research innovation, and a unique proposition via an ambitious Science Strategy which balances innovation against sustainability and affordability. It is divided into four sub-groups: Innovation Accelerator and Regulatory Science, Clinical Investigations and Trials, Standards and Compliance and Innovative Devices. The Innovative Devices function works to provide pre-market support and facilitates a smooth passage to market access. This is particularly aimed at innovative products across MedTech, diagnostics and digital, or where there is higher associated risk. The function will ensure that the UK has supply of new and advancing medical devices to include software as a medical device, novel implantables and diagnostics and play a significant role in developing the new Regulatory Framework for Medical Devices, including implementation and operation of specific services.

What’s the role? This role is a great opportunity to be involved in a highly innovative sector at a fascinating point in time. The medical devices legal landscape is changing significantly as the UK now has the opportunity to develop its own regulatory framework for medical devices. This is a permanent position within the Innovative Devices team. A key aspect of the role will be to support the MHRA’s work to develop a new regulatory framework for medical devices and delivery of quality service.

Key responsibilities:

  • Provide operational input into the Agency’s new regulatory framework planning, ensuring engagement across I&C in the necessary policy and contingency planning work.
  • Leading and assisting on consultation work on the new regulatory framework for devices.
  • Represent the Innovative Devices group in relevant cross Agency campaigns to ensure messages are correct from a medical devices regulatory perspective.
  • Assist in the development of policy underpinning the future regulatory framework for medical devices and communicate these to the wider Division and Agency.
  • Ensure maintenance of the list of MHRA policies and continue to ensure sound evidence base for new policy development.

Who are we looking for?

Our successful candidate will demonstrate the following:

  • Able to multi-task and balance competing priorities and react to multiple requests.
  • See the Bigger Picture - Understand the strategic drivers for your area of work. Align activities to contribute to wider organisational priorities.
  • Communicating & Influencing - Effective presentation and communication skills. Ability to manage up and down the organisation.
  • Delivering at Pace - Ensure delivery of timely quality outcomes, through providing the right resources to do the job, reviewing and adjusting performance expectations and rewarding success.

Person Specification:

Method of assessment: A=Application, T=Test, I=Interview, P=Presentation

Behaviour Criteria:

  • See the Bigger Picture - Understand the strategic drivers for your area of work. Align activities to contribute to wider organisational priorities. (A,I)
  • Communicating & Influencing - Effective presentation and communication skills. Ability to manage up and down the organisation. (A,I)
  • Delivering at Pace - Ensure delivery of timely quality outcomes, through providing the right resources to do the job, reviewing and adjusting performance expectations and rewarding success. (A,I)

Experience Criteria:

  • Excellent presentation and communication skills with the ability to concisely communicate information to groups of people. (A,I)
  • Excellent organisational skills and ability to prioritise extensive demands. (A,I)
  • Project management skills and experience preferred with the ability to work on different projects within the same time period, providing information on complex and technical matters. (A,I)

Technical Criteria:

  • Degree or equivalent qualification in a relevant discipline e.g. pharmacy, science, medical engineering, medical physics, biomaterials or healthcare professional qualification or equivalent qualifications or relevant work experience. (A)

If you would like to find out more about this fantastic opportunity, please read our Job Description and Person Specification!

Please note: The job description may not open in some internet browsers. Please use Chrome or Microsoft Edge. If you have any issue viewing the job description, please contact careers@mhra.gov.uk

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.
  • Our applications are CV blind, and our Hiring Managers will not be able to access your CV when reviewing your application.
  • Interview, which can include questions based on the Behaviour, Experience, Technical and Strengths Success Profiles.

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.

Use of AI in Job Applications

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 for more information on appropriate and inappropriate use.

If you require any disability related adjustments at any point during the process, please contact careers@mhra.gov.uk as soon as possible.

Closing date: 15th May 2026

Shortlisting date: from 18th May 2026

Interview date: week commencing 1st June 2026

If you need assistance applying for this role or have any other questions, please contact careers@mhra.gov.uk

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 required to work in laboratory settings
  • Roles that involve visiting other establishments where vaccination is required
  • Roles required to travel overseas where specific vaccination may be required.

Applicants who are successful at interview will be, as part of pre-employment screening subject to a check on the Internal Fraud Database (IFD). This check will provide information about employees who have been dismissed for fraud or dishonesty offences. This check also applies to employees who resign or otherwise leave before being dismissed for fraud or dishonesty had their employment continued. Any applicant’s details held on the IFD will be refused employment. A candidate is not eligible to apply for a role within the Civil Service if the application is made within a 5 year period following a dismissal for carrying out internal fraud against government.

Any move to the MHRA from another employer will mean you can no longer access childcare vouchers. This includes moves between government departments. You may however be eligible for other government schemes, including Tax-Free Childcare. Determine your eligibility here.

Individuals appointed on level transfer will retain their existing salary and are responsible for ensuring they fully understand the financial implications of any potential move and the impact (if any) on their terms. If an individual is in any doubt, they should seek clarification before accepting a job offer.

Staff joining on promotion will receive up to a 10% increase of their current basic salary, or the pay band minimum, whichever is the greater. The individual will not retain any allowances paid by the former department/Agency, unless there are special circumstances, such as a reserved right to those allowances on transfer.

Successful candidates may be subject to annual Occupational Health reviews dependent on role requirements. If you have any queries, please contact careers@mhra.gov.uk.

In accordance with the Civil Service Commissioners’ Recruitment Principles our recruitment and selection processes are underpinned by the requirement of selection for appointment on the basis of merit by a fair and open competition. If you feel your application has not been treated in accordance with the Recruitment Principles and you wish to make a complaint, you should firstly contact careers@mhra.gov.uk. If you are not satisfied with the response you receive, you can contact the Civil Service Commission at: civilservicecommission.independent.gov.uk info@csc.gov.uk Civil Service Commission Room G/8 1 Horse Guards Road London SW1A 2HQ

IVD and Medical Devices Advisor in London 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 development, flexible hybrid working arrangements, and a focus on innovation in the medical devices sector, MHRA provides its staff with meaningful opportunities to contribute to public health while fostering a collaborative and supportive culture. Join us to be part of a team that is shaping the future of healthcare regulation and making a real difference in people's lives.
Medicines and Healthcare Products Regulatory Agency

Contact Detail:

Medicines and Healthcare Products Regulatory Agency Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land IVD and Medical Devices Advisor in London

✨Tip Number 1

Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by researching the company and its recent projects. Show them you’re genuinely interested in their work and how you can contribute to their goals.

✨Tip Number 3

Practice your communication skills! Whether it’s presenting your ideas or answering questions, being clear and confident can make a huge difference in how you’re perceived.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take that extra step!

We think you need these skills to ace IVD and Medical Devices Advisor in London

Regulatory Framework Development
Policy Development
Consultation Skills
Communication Skills
Presentation Skills
Project Management
Organisational Skills
Multi-tasking
Strategic Thinking
Stakeholder Engagement
Evidence-Based Decision Making
Adaptability
Technical Knowledge in Medical Devices
Collaboration Skills

Some tips for your application 🫡

Read the Job Description Carefully: Before you start your application, take a good look at the job description. It’s packed with info about what we’re looking for, so make sure you understand the key responsibilities and person specification. This will help you tailor your application to show us why you're the perfect fit!

Be Specific in Your Examples: When answering the competency-based questions, don’t just say you have the skills; show us! Use specific examples from your past experiences that demonstrate how you meet the criteria. This is your chance to shine, so make it count!

Keep It Clear and Concise: We love a well-structured application! Make sure your answers are clear and to the point. Avoid jargon unless it’s relevant, and remember, less is often more. We want to see your skills, not wade through unnecessary fluff.

Apply Through Our Website: Don’t forget to submit your application through our website! It’s the easiest way for us to keep track of everything. Plus, it ensures you’re following the right process, which can save you time and hassle down the line.

How to prepare for a job interview at Medicines and Healthcare Products Regulatory Agency

✨Know Your Stuff

Make sure you’re well-versed in the latest regulations and innovations in medical devices. Brush up on the UK’s new regulatory framework and be ready to discuss how it impacts the industry. This shows you’re not just interested in the role, but also passionate about the field.

✨Showcase Your Communication Skills

Since effective communication is key for this role, prepare examples of how you've successfully communicated complex information in the past. Think about times when you’ve had to influence stakeholders or present to groups, and be ready to share those stories.

✨Demonstrate Your Organisational Skills

With the need to juggle multiple projects, highlight your organisational abilities. Prepare to discuss specific tools or methods you use to prioritise tasks and manage competing deadlines. This will show that you can deliver quality outcomes under pressure.

✨Align with Their Vision

Understand the strategic drivers behind the role and the organisation's goals. Be prepared to discuss how your skills and experiences align with their mission to enhance public health through innovative medical devices. This will demonstrate that you see the bigger picture.

IVD and Medical Devices Advisor in London
Medicines and Healthcare Products Regulatory Agency
Location: London

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