AI Airlock Regulations Technical Lead (Maternity Cover) in London

AI Airlock Regulations Technical Lead (Maternity Cover) in London

London Temporary 55000 - 65000 € / year (est.) Home office (partial)
Medicines and Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Lead the AI Airlock project, ensuring compliance and innovation in medical device regulations.
  • Company: Join the Medicines and Healthcare products Regulatory Agency, enhancing public 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: Make a real impact on healthcare by shaping AI regulations and collaborating with diverse stakeholders.
  • Qualifications: Bachelor's degree in science, engineering, or medicine; leadership and regulatory experience required.

The predicted salary is between 55000 - 65000 € 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 AI Airlock Regulatory Lead to join our Innovative Devices function within the Innovation and Compliance group. This is a full-time opportunity, on a 12 month fixed term contract, internal move, loan or temporary promotion 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 Software and AI Team is responsible for taking all reasonable steps to protect the public health and safeguard the interests of patients by ensuring that software as a medical device (SaMD) meet all appropriate standards of safety and performance and to encourage safe use. The Group does this by providing technical support and advice to the Policy Group; contributes to the review of clinical investigations and compliance activity; and engages with internal and external stakeholders on a range of issues involving software as a medical device.

What’s the role? A key aspect of the role will be to support the MHRA’s work in understanding how to update our regulatory framework to account for AI as a medical device. This is an important role acting as a lead for AI-Airlock and the primary interface with associated project stakeholders. There are three core elements to this role:

  • To serve as the lead on technical and regulatory expertise for the AI-Airlock project;
  • To work with colleagues within the project team, innovative devices and across the MHRA to take forward the AI Airlock project;
  • To ensure the delivery of the AI Airlock project objectives, working alongside operational expertise and management.

Key responsibilities:

  • Lead on the delivery of the AI Airlock programme. Engaging with academic networks, developers of AI, regulatory experts and clinicians to understand and address key technical regulatory challenges across different therapeutic areas and AI technologies. The post-holder must therefore possess technical knowledge of current regulations as they apply to software and AI, and familiarity or expertise with software and AI technology.
  • The postholder will possess demonstrable experience of the development of regulatory policy in the healthcare space.
  • Identify AI workstreams across the Agency and government, spot opportunities and collaborate to break down silos.
  • Lead the team of technical case managers and support engagement with innovators.

Who are we looking for? Our successful candidate will demonstrate the following:

  • Leadership - A proven leader, visible, empowering others, building resilience, and leading improvements.
  • Seeing the Big Picture – ensure plans and activities in your area of work reflect wider strategic priorities and communicate effectively with senior leaders to influence future strategies. Bring together views, perspectives, and diverse needs of stakeholders to gain a broader understanding of the issues surrounding policies and activities.
  • Working together - Works effectively as part of a multi-disciplinary team to maintain positive working relationships, working across boundaries and adding value through strategic thinking.
  • Bachelor’s degree in a relevant discipline e.g. science, engineering, medicine or equivalent experience developed through previous roles.
  • Demonstrable understanding of relevant directives and regulations, particularly UK MDR 2002 and SaMD guidance.

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

Behaviour Criteria:

  • Leadership - A proven leader, visible, empowering others, building resilience, and leading improvements. (A, I)
  • Seeing the Big Picture – ensure plans and activities in your area of work reflect wider strategic priorities and communicate effectively with senior leaders to influence future strategies. Bring together views, perspectives, and diverse needs of stakeholders to gain a broader understanding of the issues surrounding policies and activities. (A, I)
  • Working together - Works effectively as part of a multi-disciplinary team to maintain positive working relationships, working across boundaries and adding value through strategic thinking. (A, I)

Experience Criteria:

  • Demonstrable experience of effective use of resources to meet agreed workload priorities and allocation of staff. (A, I)
  • Extensive and proven ability to work with discretion and capability in own area, providing effective support and specialist advice. (A, I)
  • Proven ability of leading projects/investigations and liaising with stakeholders e.g. DHSC, Approved Bodies and Industry (A, I)
  • Excellent written and oral communication skills including grammatical/technical writing skills (A, I)

Technical Criteria:

  • Bachelor’s degree in a relevant discipline e.g. science, engineering, medicine or equivalent experience developed through previous roles. (A, I)
  • Demonstrable understanding of relevant directives and regulations, particularly UK MDR 2002 and SaMD guidance. (A, I)
  • Ability to interpret new regulatory concepts and to apply to existing and future regulatory frameworks. (A, I)

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.

In the instance that we receive a high number of applications, we will hold an initial sift based on the lead criteria of:

  • Leadership
  • 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.

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: 31st May 2026

Shortlisting date: from 1st June 2026

Interview date: week commencing 8th 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

AI Airlock Regulations Technical Lead (Maternity Cover) 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 public health and innovation, employees benefit from a flexible hybrid working model, opportunities for professional growth, and the chance to contribute to groundbreaking regulatory frameworks in AI and medical devices. The collaborative culture fosters teamwork across diverse disciplines, ensuring that every team member's voice is valued and heard.

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 AI Airlock Regulations Technical Lead (Maternity Cover) in London

Tip Number 1

Network like a pro! Reach out to people in the industry, especially those connected to the MHRA or AI regulations. A friendly chat can open doors and give you insights that might just set you apart from other candidates.

Tip Number 2

Prepare for the interview by brushing up on your knowledge of UK MDR 2002 and SaMD guidance. Be ready to discuss how your experience aligns with the role's requirements. We want to see your passion for innovation and compliance!

Tip Number 3

Showcase your leadership skills during the interview. Think of examples where you've empowered others or led a project successfully. We love candidates who can inspire and drive improvements within a team!

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we’re all about making the process as smooth as possible for you.

We think you need these skills to ace AI Airlock Regulations Technical Lead (Maternity Cover) in London

Technical Knowledge of AI and Software Regulations
Regulatory Policy Development
Stakeholder Engagement
Leadership Skills
Strategic Thinking
Multi-disciplinary Team Collaboration
Understanding of UK MDR 2002

Some tips for your application 🫡

Read the Job Description Carefully:Before you start writing, make sure to read the job description thoroughly. It’s packed with clues about what the hiring team is looking for, so highlight key responsibilities and skills that match your experience.

Tailor Your Application:Don’t just send a generic application! Tailor your responses to reflect how your skills and experiences align with the specific requirements of the AI Airlock Regulations Technical Lead role. Use the same language as the job description to show you’re a perfect fit.

Be Clear and Concise:When answering application questions, keep it clear and to the point. Use bullet points if necessary to make your achievements stand out. Remember, clarity is key in showcasing your qualifications!

Apply Through Our Website:We encourage you to apply through our website for a smooth application process. Make sure all sections are filled out completely, as incomplete applications might not be considered. Good luck!

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

Know Your Regulations

Make sure you brush up on the UK MDR 2002 and SaMD guidance. Being able to discuss these regulations confidently will show that you understand the framework you'll be working within, which is crucial for the AI Airlock role.

Showcase Your Leadership Skills

Prepare examples of how you've led teams or projects in the past. This role requires a proven leader, so think about times when you've empowered others or driven improvements. Be ready to share specific outcomes from your leadership.

Engage with Stakeholders

Think about how you've worked with diverse stakeholders in previous roles. Be prepared to discuss how you’ve built relationships and collaborated across boundaries, as this will be key in engaging with academic networks and clinicians.

Communicate Clearly

Practice articulating complex ideas simply and clearly. You’ll need excellent written and oral communication skills, so consider preparing a brief presentation on a relevant topic to demonstrate your ability to convey technical information effectively.