Regulatory Specialist - Medical Devices

Nottingham, United Kingdom | Posted on 13/02/2026

This is an opportunity to take meaningful ownership of regulatory activities at a pivotal stage in agrowing medical device company.

Neupulse is moving fromdevelopment into delivery. Our technology is designed to improve quality oflife for people with Tourette Syndrome, and we are now progressing through keyregulatory milestones as we prepare to scale internationally.

We’re looking for a Regulatory Specialist who wants real responsibility — someone motivated by owningoutcomes, applying judgement, and building on solid foundations as the organisation grows.

This role is about accountability and influence , not just process execution.

Regulatory structures and activities are already in place and progressing. Your role is to take ownership of these foundations, strengthen them, and help ensure they scaleeffectively as Neupulse moves through approvals and into commercial delivery.

You’ll work closely with engineering, clinical, and leadership teams, and act as a central point ofcontact with regulators, notified bodies, and external partners.

• take ownership of regulatory activities across the product lifecycle
• lead and manage regulatory submissions and approvals,particularly for Class II medical devices
• support and manage compliance with EU MDR and relevant FDA pathways
• interpret regulatory requirements pragmatically and applythem to a growing organisation
• maintain and develop the Quality Management System (e.g. ISO
  13485)
• act as the primary interface with regulators, notifiedbodies, and external partners
• support audits, post-market surveillance, and ongoing compliance activities
• buildon existing regulatory foundations and help them scale as the company grows

This is a hands-onrole, combining strategic thinking with practical execution.

This role tends to suitpeople who:

• wantto own the regulatory function , not just contribute to it
• enjoy shaping how things are done as organisations grow
• value applying judgement over following rigid templates
• want visibility, influence, and impact within a smallercompany
• are motivated by working on products that make a real difference to users

You’ll have the opportunity to make thoughtful improvements, establish credibility withregulators, and help set the direction for regulatory work as the businessscales.

This role is a strongfit for someone who:

• has a Bachelor’s degree in Life Sciences, Engineering, Biomedical Sciences, or related field
• has 2+ years of hands-on Regulatory Affairs experience with Class II medical devices
• has worked with medical device regulations such as EU MDR and/or FDA
• understands regulatory submissions and quality systems end toend
• is comfortable working in a smaller, less hierarchicalorganisation
• enjoys building on existing regulatory foundations and helping them scale
• can balance regulatory rigour with commercial and operationalrealities
• enjoysbeing accountable for outcomes, not just inputs

What matters most iscapability, judgement, and the motivation to take ownership at a criticalstage.

Neupulse is a UK-basedhealth technology company developing innovative solutions to help people with Tourette Syndrome better manage their symptoms. The team combines technicaldepth with a strong sense of purpose and real-world user impact.

This role is based full time in Nottingham. Candidates must already have the unrestricted right to work in the UK, as Neupulse is not able to offer visa sponsorship for this position.

If this sounds like arole where you’d enjoy taking ownership, applying your judgement, and helping agrowing medical device company scale responsibly, we’d love to start aconversation.

Interested, but want to learn more first?

Neupulse is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees.