Regulatory Affairs Specialist, Medical Devices
2 settimane fa
A medical device manufacturer is seeking a Regulatory Affairs Specialist to assist in registering medical devices in EXTRA-CEE countries. Responsibilities include preparing regulatory documents, managing submissions, and ensuring compliance with EU regulations. The ideal candidate should have a Bachelor's degree in a scientific discipline and at least 3 years of experience in regulatory affairs in the medical device industry. Fluency in English is required for effective communication. J-18808-Ljbffr
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Regulatory Affairs Specialist
2 settimane fa
Uri (SS), Italia Whatjobs A tempo pienoMECTRON SPA, A DESIGNER AND MANUFACTURER OF DENTAL AND MEDICAL DEVICES IS LOOKING FOR Regulatory Affairs Specialist The Regulatory Affairs Specialist assists the Senior Regulatory Affairs Manager in the registration of medical devices in EXTRA-CEE countries following a plan that is constantly updated in accordance with company strategy. Essential Duties and...
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Regulatory Affairs Specialist, Medical Devices
2 settimane fa
Uri, Italia Whatjobs A tempo pienoA medical device manufacturer is seeking a Regulatory Affairs Specialist to assist in registering medical devices in EXTRA-CEE countries. Responsibilities include preparing regulatory documents, managing submissions, and ensuring compliance with EU regulations. The ideal candidate should have a Bachelor's degree in a scientific discipline and at least 3...
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Regulatory Affairs Specialist
3 settimane fa
Uri, Italia Whatjobs A tempo pienoMECTRON SPA, A DESIGNER AND MANUFACTURER OF DENTAL AND MEDICAL DEVICES IS LOOKING FOR Regulatory Affairs Specialist The Regulatory Affairs Specialist assists the Senior Regulatory Affairs Manager in the registration of medical devices in EXTRA-CEE countries following a plan that is constantly updated in accordance with company strategy. Essential Duties and...
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Senior Regulatory Affairs Consultant
3 giorni fa
Uri, Italia Rebell Ag A tempo pienoDescrizione del posto vacanteSei pronto per entrare a far parte di unasocietà di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device?PQE Group è affermata in questo settoredal ****, garantendo una presenza internazionale grazie alle45 filialie i**** dipendentiin Europa, Asia e nelle Americhe.Lavorare in una realtà di consulenza...
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Regulatory Affairs
2 settimane fa
Uri, Italia Whatjobs A tempo pienoPRODECO PHARMA opera da più di 35 anni nel campo della salute proponendo un solido listino di prodotti fitoterapici (dispositivi medici ed integratori alimentari).Siamo una realtà dinamica, con una forte propensione all'innovazione e alla ricerca, presente sul territorio nazionale in quasi **** punti vendita selezionati tra farmacie, parafarmacie ed...
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Regulatory Affairs Dispositivi Medici
2 settimane fa
Uri, Italia Whatjobs A tempo pienoUn'azienda nel settore salute cerca un Regulatory Affairs specializzato in dispositivi medici.Il candidato dovrà gestire le attività regolatorie, come la redazione della documentazione necessaria e la verifica delle normative di settore.È necessaria una laurea in discipline scientifiche e almeno 2 anni di esperienza nel settore.Richieste ottime doti...
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Senior Regulatory Affairs Lead
3 giorni fa
Uri, Italia Rebell Ag A tempo pienoUna società di consulenza farmaceutica cerca un Senior Regulatory Affairs con 5-7 anni di esperienza in ambito Regulatory Affairs.La persona selezionata coordinerà attività regolatorie e supporterà lo sviluppo dei progetti, garantendo conformità con le normative.Si richiede laurea in disciplina scientifica e ottima conoscenza dell'inglese.L'offerta...
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Senior Embedded Firmware Engineer — Medical Devices
1 settimana fa
Uri, Italia Altro A tempo pienoSenior Firmware Engineer needed to design, implement, and test embedded software for medical devices, ensuring IEC ***** Class C compliance.Requires experience in embedded software development and leading teams.
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Senior Embedded Firmware Engineer — Medical Devices
2 settimane fa
Uri, Italia Livanova A tempo pienoA global medtech company is seeking a Senior Firmware Engineer to design and implement embedded software for Heart-Lung Machines and other medical devices.You will mentor junior engineers, ensure compliance with safety and regulatory standards, and work on real-time systems using C/C++.This full-time position offers a chance to innovate in a collaborative...
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Clinical Data Administrator
1 settimana fa
Uri, Italia Planet Pharma A tempo pienoTitle: Clinical Data Administrator - Data EntryLocation: La Spezia, ItalyClient: Leading CROType: 2-3 months contract - 20 hours per weekMain ResponsibilitiesEnter clinical study data into the designated system accurately and efficientlyReview source documents and extract relevant clinical informationCollaborate professionally with site staff, physicians,...