Regulatory Consultant – Electronic Medical Devices (IEC 60601 Focus)
Remote (UK or Ireland based) | Circa £60,000 – £70,000+
* Applicants must have the right to work in the UK or Ireland and either already be residing there or have a clear, committed plan to relocate.
* This role requires in-depth experience in regulatory affairs within active (electronic) medical devices.
* Applicants with detailed experience in electronic medical device development seeking a higher salary will also be considered.
What if your next role offered both freedom and real impact?
You start the day from home, coffee in hand, dialling into a call with a MedTech founder. Their product is a connected therapeutic device set to transform remote care, but they need help navigating the regulatory landscape.
You listen, ask the right questions, and offer clear, practical guidance that keeps their innovation on track without losing pace.
That afternoon, a different challenge: reviewing documentation for a scaling company preparing their first FDA submission.
You’ve seen where this can go wrong, and you know how to steer it right. You spot the gaps, help tighten the strategy, and give the client the confidence they need.
It’s varied, meaningful work — delivered with autonomy and backed by a team of experts.
At IMed Consultancy, no two weeks look the same.
You might be helping one client plan market entry into the US, supporting another with MDR strategy for a Class IIb platform, and advising a third on post-market obligations. The common thread? Trusted relationships and technically ambitious projects.
You’ll join a tight-knit team of 11 consultants. Each brings something different, but everyone works collaboratively. There’s no red tape — just good people doing great work.
What You’ll Do
Projects vary depending on each client’s needs, but typically include:
• Leading and supporting EU MDR and US FDA submissions
• Guiding clients on regulatory strategy across the full product lifecycle
• Building and reviewing technical documentation, from DHF to CERs
• Contributing to risk management, usability, and clinical evaluation planning
• Supporting post-market compliance and global market access strategy
• Acting as a trusted advisor to startups and scaling MedTech companies
What You’ll Bring
• Regulatory experience with active or electronic medical devices
• Strong understanding of MDR and FDA pathways
• Detailed knowledge of IEC 60601 and a desire to deepen that specialism
• Confidence working with technical teams and senior stakeholders
• A pragmatic, commercially minded approach to problem-solving
What You’ll Get
• £60,000 – £70,000+ basic salary (or equivalent in Euros for Ireland-based applicants)
• Applicants with in-depth experience of electronic medical device development seeking a higher salary will also be considered
• Fully remote role (UK or Ireland based)
• Varied, high-impact project work
• Real development opportunities — in consulting and beyond
• A supportive, expert team that shares your standards
About IMed Consultancy
IMed is a specialist RA/QA consultancy founded in 2012, known for helping innovative MedTech companies bring devices to market across the UK, EU, and US. From digital health to complex electro-mechanical systems, we simplify regulatory complexity and enable innovation.
Interested?
Indo Search is representing IMed on an exclusive basis.
Get in touch with Josh Craven at josh@indoprofessionals.co.uk or 07929 235128.