Regulatory Affairs Associate – Medical Devices
6 giorni fa
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 interested in this opportunity, please reach out for more details.#J-18808-Ljbffr
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Regulatory Affairs Specialist
1 settimana fa
Rome, Italia Altro A tempo pienoRegulatory Affairs Specialist -Medical Devices Join to apply for the Regulatory Affairs Specialist -Medical Devices role at Nordberg MedicalRegulatory Affairs Specialist -Medical Devices Join to apply for the Regulatory Affairs Specialist -Medical Devices role at Nordberg MedicalGet AI-powered advice on this job and more exclusive features.The Regulatory...
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Regulatory Affairs Specialist
1 settimana fa
Rome, Italia Altro A tempo pienoRegulatory Affairs Specialist -Medical DevicesJoin to apply for theRegulatory Affairs Specialist -Medical Devicesrole atNordberg Medical Regulatory Affairs Specialist -Medical DevicesJoin to apply for theRegulatory Affairs Specialist -Medical Devicesrole atNordberg Medical Get AI-powered advice on this job and more exclusive features. TheRegulatory Affairs...
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Rome, Italia Resourcing Life Science A tempo pienoWhat 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...
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Medical Affairs Director
4 settimane fa
Rome, Italia Altro A tempo pienoAre you passionate about bringing new pharmaceutical products to patients? Do you have solid Medical Affairs experience and the drive to lead and further develop the Medical Affairs function in Italy? If so, we are looking for a new Medical Affairs Director to take over this important role at Ascendis PharmaAscendis Pharmais a global biopharmaceutical...
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Regulatory Affairs Specialist
7 giorni fa
Rome, Italia Named S.r.l. A tempo pienoIl 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...
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Senior Technical Reviewer, Active Medical Devices
2 settimane fa
Rome, Italia Altro A tempo pienoA 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....
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Rome, Italia Lavoropiu Spa A tempo pienoFarmapiù 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-...
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Regulatory Affairs Manager
2 settimane fa
Rome, Italia Scienta A tempo pienoDirect message the job poster from ScientaPartnering with CDMOs to strengthen their Commercial TeamsWe'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...
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Regulatory affairs cmc
2 settimane fa
Rome, Italia Dompé A tempo pienoDompé farmaceutici is an international biopharmaceutical company involved in all activities of the pharmaceutical value chain, from research to development, production and marketing.For our office in L'Aquila we are looking for a Regulatory Affairs CMC & Site Regulatory. The Regulatory Affairs CMC & Site Regulatory Specialist manages regulatory bodies,...
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Technical Reviewer
2 settimane fa
Rome, Italia Altro A tempo pienoGreat that you're thinking about a career with BSI!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. BSI is seeking experienced R&D Engineers to join our Active Medical Devices team as a home-based Technical Specialist & Scheme Manager (Technical...