Lavori attuali relativi a Ra Specialist Medical Devices - Milano - Page Personnel
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Ra Specialist Medical Devices
3 settimane fa
Milano, Italia Page Personnel A tempo pienoWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team.The Regulatory Affairs Specialist will play a key role in ensuring compliance with regulatory requirements for our medical devices.This individual will collaborate cross-functionally with internal teams to support product development, registration, and...
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Ra Specialist Medical Devices
1 mese fa
Milano, Italia Page Personnel A tempo pienoIl nostro cliente Medical company that develops Class III, II and I devices La figura ricercata We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team. The Regulatory Affairs Specialist will play a key role in ensuring compliance with regulatory requirements for our medical devices. This individual will...
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Ra Specialist Medical Devices
2 mesi fa
Milano, Italia Page Personnel A tempo pienoIl nostro cliente Medical company that develops Class III, II and I devices La figura ricercata We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team. The Regulatory Affairs Specialist will play a key role in ensuring compliance with regulatory requirements for our medical devices. This individual will...
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Design Control Specialist
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Design Control Specialist
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Milano, Italia Novasyte A tempo pienoOur client, Chiesi Farmaceutici - one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry - in order to expand their staff, entrusted to IQVIA the recruitment of Design Control Specialist - Medical Devices - who can join an exciting working environment in a dynamic...
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Tender Specialist
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Regulatory Affairs Specialist for Medical Devices
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Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist for Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our team in ensuring compliance with regulatory requirements for our medical devices.Prepare and submit regulatory submissions to regulatory authorities, including 510(k) premarket notifications, Technical Files,...
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Regulatory Affairs Specialist for Medical Devices
3 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist for Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to play a key role in ensuring compliance with regulatory requirements for our medical devices.This individual will collaborate cross-functionally with internal teams to support product development, registration, and...
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Milano, Lombardia, Italia Page Personnel A tempo pienoJob SummaryWe are seeking a highly motivated Regulatory Affairs Specialist to support our medical devices team.Main ResponsibilitiesAs a Regulatory Affairs Specialist, you will play a key role in ensuring compliance with regulatory requirements for our medical devices. Key responsibilities include preparing and submitting regulatory submissions to regulatory...
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Regulatory Affairs Specialist Medical Devices
4 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our medical device team.Key Responsibilities:Prepare and submit regulatory submissions to regulatory authorities, including 510(k) premarket notifications, Technical Files, Design Dossiers, and other regulatory filings...
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Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our medical device team. The successful candidate will play a key role in ensuring compliance with regulatory requirements for our medical devices.Key Responsibilities:Regulatory Submissions: Prepare and submit...
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Regulatory Affairs Specialist Medical Devices
4 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our medical device team. The successful candidate will play a key role in ensuring compliance with regulatory requirements for our medical devices.Key Responsibilities:Regulatory Submissions: Prepare and submit...
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Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at Page Personnel. The successful candidate will play a key role in ensuring compliance with regulatory requirements for our medical devices.Key Responsibilities:Regulatory Submissions: Prepare and submit...
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Regulatory Affairs Specialist Medical Devices
4 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at Page Personnel. The successful candidate will play a key role in ensuring compliance with regulatory requirements for our medical devices.Key Responsibilities:Regulatory Submissions: Prepare and submit...
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Regulatory Affairs Specialist Medical Devices
2 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist Medical DevicesPage Personnel è alla ricerca di un Regulatory Affairs Specialist Medical Devices motivato e dettagliato per unirsi al nostro team. Il Regulatory Affairs Specialist Medical Devices svolgerà un ruolo chiave nell'assicurare la conformità con i requisiti regolatori per i dispositivi medici. Questo individuo...
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Regulatory Affairs Specialist for Medical Devices
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Milano, Lombardia, Italia Page Personnel A tempo pienoRegulatory Affairs Specialist for Medical DevicesWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our medical device team. The ideal candidate will have a strong understanding of regulatory requirements and guidelines, including FDA regulations (21 CFR Part 820), ISO 13485, and other applicable standards.Key...
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Regulatory Affairs Specialist Medical Devices
5 giorni fa
Milano, Lombardia, Italia Page Personnel A tempo pienoAbout the RoleWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our client, a medical company that develops Class III, II, and I devices.Key ResponsibilitiesRegulatory SubmissionsPrepare and submit regulatory submissions to regulatory authorities, including 510(k) premarket notifications, Technical Files, Design...
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Production Specialist
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Milano, Lombardia, Italia Tensive A tempo pienoJob DescriptionTensive, a leading biomedical startup, is seeking a highly skilled Production Specialist to join our team. In this role, you will be responsible for supporting production and quality control activities in our ISO 7 cleanroom, where we develop innovative prostheses for breast reconstruction and augmentation.We are looking for a collaborative...
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Regulatory Affairs Specialist
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Milano, Italia Hunters Group A tempo pienoPer azienda cliente, realtà leader nel settore farmaceutico e cosmetico in Italia, siamo alla ricerca di una figura di Regulatory Affairs Specialist - Medical Devices.Redigere e aggiornare la documentazione relativa alla legislazione e alle linee guida degli enti regolatori nazionali ed internazionali con cui ci si interfaccia; Assicurare la conformità del...
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Regulatory Affairs Specialist for Medical Devices
2 settimane fa
Milano, Lombardia, Italia Page Personnel A tempo pienoJob DescriptionWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support our medical device team.The successful candidate will play a key role in ensuring compliance with regulatory requirements for our medical devices.This individual will collaborate cross-functionally with internal teams to support product development,...
Ra Specialist Medical Devices
2 mesi fa
- RA Specialist Medical Devices - Medical company that develops Class III, II and I devices Il nostro clienteMedical company that develops Class III, II and I devicesRuoloWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team.
