Regulatory Affairs Specialist, Medical Devices

A leading health technology company in Greater London is seeking a Regulatory Affairs Specialist. This role involves supporting regulatory pathways for medical devices and ensuring compliance with global standards. You will collaborate across teams, prepare regulatory submissions, and monitor evolving requirements. Ideal candidates have 3–6 years of...

A health technology company based in London seeks a Regulatory Affairs Specialist to ensure compliance with global regulatory requirements. The role involves supporting regulatory submissions, translating regulatory standards, and collaborating with cross-functional teams. Ideal candidates have 3-6 years of regulatory experience in medical devices and strong...

About SAVAAll the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real-time and affordable way.The RoleAt SAVA, we are building next-generation biosensors...

A global medical technology company is seeking a Principal Regulatory Affairs Specialist to lead regulatory submissions and ensure compliance for medical devices. The role involves preparing regulatory dossiers, interacting with authorities, and recommending improvements for processes. Candidates should have experience with UK MHRA submissions and a strong...

Choose LocationChoose Location# Director, Regulatory Affairs (Digital Medical Devices)REQ-10064222Nov 10, 2025United Kingdom### Summary#LI-Hybrid (12 days per month on-site) Location: London (The Westworks), United Kingdom We’re looking for a seasoned regulatory expert to lead global strategy and execution for digital medical devices, including Digital...

**Summary**: LI-Hybrid (12 days per month on-site) Location: London (The Westworks), United Kingdom The Associate Director, Regulatory Affairs (Medical Devices) independently provides strategic and operational global medical device regulatory direction and documentation for projects/products covering design and development, registration, approval and post...

About SAVA All the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real‑time and affordable way. The Role At SAVA, we are building next-generation...

A leading healthcare technology company is seeking a Regulatory Affairs Specialist to oversee regulatory submissions and compliance processes. This role requires experience in medical device regulations, particularly with UK MHRA and CE/UKCA marking. The ideal candidate will excel in technical writing and possess a deep understanding of EU MDR and risk...

Job Description Summary Office Location: London (The Westworks), United Kingdom #LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office) #LI-Remote Remote (if living beyond 50 miles to our London office) The Associate Director, Regulatory Affairs (Medical Devices) independently provides strategic and operational global...

Job Description SummaryTake the next step in your career now, scroll down to read the full role description and make your application.Office Location: London (The Westworks), United Kingdom#LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office)#LI-Remote Remote (if living beyond 50 miles to our London office)The Associate...