Freelance EU MDR Regulatory Lead for Medical Devices

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...

Senior Clinical Medical Device Consultant We are seeking a freelance Senior Clinical Medical Device Consultant who has experience conducting regulatory strategies for clinical trial start‑up activities in a variety of European countries, including the UK and Germany. The candidate should also be experienced with authoring and reviewing clinical...

Senior Clinical Medical Device Consultant We are seeking a freelance Senior Clinical Medical Device Consultant who has experience conducting Regulatory strategies for clinical trial start up activities for a variety of European countries including UK & DE. They should also be experienced with authoring and reviewing clinical documentation to ensure...

Company Description SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We...

Opportunity to join a Medical Device-focused CRO and provide market-leading writing support. **The Company:** An international CRO that accelerates product development through integrated laboratory, clinical and consulting services. They provide holistic support to clients from development to commercialization. Now in a period of growth, they are seeking...

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 a Innovative Devices Regulation Lead to...

Director, Regulatory Affairs, Pre-MarketJob Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. Interprets simple internal and external...

A global healthcare technology leader is seeking a Principal Regulatory Affairs Specialist for their Diabetes division in Greater London. This role involves coordinating regulatory submissions, leading compliance activities, and ensuring adherence to regulatory requirements. Candidates should have a strong background in medical device regulatory affairs,...

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...

Opportunity to join a Medical Device manufacturer and provide market-leading Medical Writing support. **Senior Medical Writer Role:** - Conduct scientific literature reviews and compile reports, including annual literature updates and periodic safety updates, to provide to global regulatory agencies - Attends stakeholder meetings (internal and external)...