Medical Device Regulatory Affairs Specialist

Medical Device – Regulatory Affairs DirectorResponsibilitiesLine management of 10 Regulatory Line ManagersEstablish and implement regulatory strategies ensuring new and existing products comply with the latest global requirementsTrain the team on EMEA / FDA requirementsQualificationsMinimum 8 years in regulatory affairs in the medical device...

Medical Device – Regulatory Affairs Director Responsibilities Line management of 10 Regulatory Line Managers Establish and implement regulatory strategies ensuring new and existing products comply with the latest global requirements Train the team on EMEA / FDA requirements Qualifications Minimum 8 years in regulatory affairs in the medical device industry...

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...

Role DescriptionLine management 10 Regulatory Line ManagersEstablish and implement regulatory strategies ensuring new and existing products comply with the latest global requirements.Training the team with EMEA / FDA requirementsQualificationsMin 8 years in regulatory affairs in medical deviceMin 4 years as Regulatory Affairs Manager / DirectorExperience...

Get AI-powered advice on this job and more exclusive features.Sentinel Diagnostics, leader in the Development and Production of Diagnostic Kits for Clinical Chemistry, Immunology, Molecular Biology, Chromatography and Rapid Test, in order to expand the Regulatory Affairs Team, is looking for a:REGULATORY AFFAIRS SPECIALISTResponsibilitiesDefinition of...

A leading medical device firm in Italy is seeking a Regulatory Affairs professional to support CE marking activities for medical devices. The role involves ensuring regulatory compliance, developing strategies, and collaborating with cross-functional teams. Ideal candidates will have 3-5 years of experience in Regulatory Affairs and possess a good...

A leading medical diagnostics firm based in Milan is seeking a Regulatory Affairs Specialist to join their team. The ideal candidate will have a Scientific Degree and at least 3-4 years of experience in the Medical Device/IVD sector. Responsibilities include defining regulatory strategies for global market access, preparing necessary documentation for...

: Quality Assurance **Posizione: Regulatory Affairs & Clinical Specialist** **Location: Milano provincia (on-site)** **Retribuzione: commisurata all'effettiva esperienza** Siamo alla ricerca di un Regulatory Affairs & Clinical Specialist per conto di un'azienda storica, basata in provincia di Milano. Si tratta di un'azienda fabbricante di Medical...

A global healthcare company based in Italy seeks a Non-Pharma Global Regulatory Affairs Specialist to manage regulatory documentation for projects in compliance with EU regulations. The role involves collaboration with internal teams and contributes to regulatory strategies for new projects. Candidates should have at least 5 years of experience in Regulatory...

A global healthcare consulting firm is seeking an experienced Regulatory Affairs professional specializing in in vitro diagnostics (IVD) and Companion Diagnostics (CDx). This role involves developing regulatory strategies, collaborating with cross-functional teams, and managing submissions for regulatory approvals. Candidates must have at least 5 years in...