Regulatory Affairs Lead – Medical Devices

Regulatory Affairs Specialist -Medical DevicesJoin to apply for theRegulatory Affairs Specialist -Medical Devicesrole atNordberg MedicalRegulatory Affairs Specialist -Medical DevicesJoin to apply for theRegulatory Affairs Specialist -Medical Devicesrole atNordberg MedicalGet AI-powered advice on this job and more exclusive features.TheRegulatory Affairs...

A life sciences recruitment firm is seeking a Regulatory Affairs professional with at least 4 years of experience in the medical device sector.The role involves conducting regulatory assessments, managing registrations, and supporting FDA submissions.Excellent communication and problem-solving skills are essential, along with fluency in English.If you are...

The Director of Regulatory Affairs leads the global regulatory strategy of the MedTech AI Division, ensuring that all software and hardware products (SaMD, AI-enabled real-time systems, edge–cloud devices, imaging platforms, connectivity and data solutions) comply with U.S., EU, and international regulations.Reporting to the VP of Clinical Quality and...

What to ExpectConduct regulatory impact assessments for product changes, including determination of letter-to-file versus submission requirements.Manage annual registrations, license renewals, and ongoing regulatory notifications.Support the preparation, submission, and maintenance of FDA dossiers and related technical documentation.Coordinate the...

A leading recruitment agency is seeking a Regulatory Affairs Director in Milan, Italy.The role involves managing a team of Regulatory Line Managers and ensuring compliance with EMEA and FDA regulatory requirements.Candidates should possess over 8 years of experience in regulatory affairs within the medical device industry, with at least 4 years in a...

Sr Specialist, Global Regulatory Affairs Herbalife Italy – RomeVia Amsterdam, 125Roma*****About the roleWe're looking for an experienced Senior Specialist, Global Regulatory Affairs to join our dynamic Global Regulatory Affairs team, supporting the Europe & Africa (E&A) sub-region.This role is based in Rome, Italy and plays a key part in ensuring the...

A premier certification body is seeking a home-based Technical Specialist & Scheme Manager to evaluate medical devices for compliance and support manufacturers throughout their certification life cycle.The position requires at least 5 years of experience with active medical devices, a relevant degree, and a deep understanding of regulatory requirements.This...

Alchimiais one of the leading European manufacturers of medical devices for ophthalmic surgery and tissue banks.With our expertise in the fields of chemistry, microbiology, and pharmacology, at Alchimia we have adopted this rule: we design each medical device as if it were intended for ourselves.Since our foundation in ****, all our products have been...

Director Medical Affairs – Region Europe Our client, a leading international pharmaceutical company, is seeking a Director Medical Affairs – Region Europe to join their European headquarters in Paris.The RoleAs Director Medical Affairs – Region Europe, you will shape and execute the regional medical strategy for the clinical nutrition and hospital care...

Partnering with CDMOs to strengthen their Commercial Teams We're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team.This is an exciting opportunity to lead end-to-end regulatory operations across a diverse portfolio of...