Remote Regulatory Specialist – Active Medical Devices

Job Title Technical Specialist & Scheme Manager - Active Devices Location Home-based position located in the UK or Europe with up to 20% travel for training. ResponsibilitiesReview and evaluate medical device technical and clinical documentation in your areas of competence to assess compliance with MDD 93 / 42 / EEC, MDR 2017 / 745 and UK MDR 2012 schemes....

Job TitleTechnical Specialist & Scheme Manager - Active DevicesLocationHome-based position located in the UK or Europe with up to 20% travel for training.ResponsibilitiesReview and evaluate medical device technical and clinical documentation in your areas of competence to assess compliance with MDD 93 / 42 / EEC, MDR 2017 / 745 and UK MDR 2012 schemes.Manage...

Il Gruppo Named , per la propria sede Named Srl di Lesmo (MB), in un’ottica di potenziamento del proprio organico, è alla ricerca di una figura di : REGULATORY AFFAIRS SPECIALIST Il candidato, inserito presso l’Ufficio Regolatorio, si occuperà di :Preparazione ed archiviazione della documentazione tecnico-regolatoria per la registrazione di prodotti...

Farmapiù Bologna, divisione specialistica del gruppo Lavoropiù, cerca un/a Regulatory Affairs Specialist Senior con almeno 5/6 anni di esperienza nel ruolo e nel settore dispositivi medici per azienda cliente, produttore biomedicale, sita a Medolla (MO).La risorsa si occuperà di Gestire le attività di registrazione in ambito UE, FDA e altri paesi extra-...

A medical technology company is seeking a remote Product Specialist in Lombardy. You will manage and grow sales, establish relationships with customers and KOLs, and support product training. A bachelor's degree and 5+ years in medical device sales in Italy is required, along with fluency in Italian and English. This role involves approximately 60% travel....

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while...

A leading medical certification firm is looking for Medical Devices Auditors and Product Reviewers to join their team in Rho, Milan, Italy. Candidates must possess a degree in engineering or relevant fields and have at least 4 years of experience in medical manufacturing. Key responsibilities include conducting technical assessments and compliance audits...

A global pharmaceutical company, located in Turbigo, Italy, is seeking a Senior Pharmacovigilance Physician. This role involves medical review of safety reports, supporting regulatory tasks, and mentoring junior staff. The ideal candidate has a medical qualification and extensive experience in pharmacovigilance with strong signal detection skills. This...

Medical Devices Auditors & Product Reviewer3 days ago Be among the first 25 applicantsDirect message the job poster from MTIC GroupCoordinator For International Relations & Marketing at MTIC GroupMTIC InterCert of MTIC Group is growing steadily and successfully in all areas of Certification, particularly as a Notified Body (CE 0068) in Medical Device...

Medical Devices Auditors & Product Reviewer 3 days ago Be among the first 25 applicants Direct message the job poster from MTIC Group Coordinator For International Relations & Marketing at MTIC Group MTIC InterCert of MTIC Group is growing steadily and successfully in all areas of Certification, particularly as a Notified Body (CE 0068) in Medical Device...