Regulatory Affairs Specialist

7 ore fa


Roma, Italia TransPerfect A tempo pieno

A medical device company in Rome is seeking a Regulatory Affairs Specialist to support CE marking activities and ensure regulatory compliance for medical devices. The ideal candidate will have 3-5 years of experience in Regulatory Affairs, strong knowledge of CE marking regulations, and excellent communication skills in English. This role involves collaboration with cross-functional teams and providing direction regarding regulatory requirements. Join us in advancing medical technology and improving patient outcomes.#J-18808-Ljbffr



  • roma, Italia Nordberg Medical A tempo pieno

    Regulatory Affairs Specialist -Medical DevicesJoin to apply for the Regulatory Affairs Specialist -Medical Devices role at Nordberg MedicalRegulatory Affairs Specialist -Medical DevicesJoin 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...


  • roma, Italia Nordberg Medical A tempo pieno

    Regulatory Affairs Specialist -Medical DevicesJoin to apply for the Regulatory Affairs Specialist -Medical Devices role at Nordberg MedicalRegulatory Affairs Specialist -Medical DevicesJoin 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...

  • Regulatory Affairs

    3 settimane fa


    Roma, Italia Claire Joster | People First A tempo pieno

    Un'agenzia di selezione di personale sta cercando un Certifications and Regulatory Affairs Specialist per garantire la conformità regolamentare dei prodotti in plastica e packaging cosmetico. La figura si occuperà di collaborare con i vari reparti aziendali e supportare lo sviluppo di nuovi prodotti, assicurando il rispetto delle normative UE e...


  • Giuliano di Roma, Italia ResMed Inc A tempo pieno

    OverviewAdvanced Regulatory Affairs Specialist – responsible for regulatory activities related to the import and distribution of ResMed products in the EMEA region, from product registrations to post‑market activities. The role involves collaborating with local regulatory partners, legal manufacturers and other functions to ensure compliance across the...


  • giuliano di roma, Italia ResMed Inc A tempo pieno

    OverviewAdvanced Regulatory Affairs Specialist – responsible for regulatory activities related to the import and distribution of ResMed products in the EMEA region, from product registrations to post‑market activities. The role involves collaborating with local regulatory partners, legal manufacturers and other functions to ensure compliance across the...


  • Giuliano di Roma, Italia ResMed Inc A tempo pieno

    Overview Advanced Regulatory Affairs Specialist – responsible for regulatory activities related to the import and distribution of ResMed products in the EMEA region, from product registrations to post‑market activities. The role involves collaborating with local regulatory partners, legal manufacturers and other functions to ensure compliance across the...


  • roma, Italia Michael Page A tempo pieno

    OverviewAzienda con attività farmaceutica: Per conto di un nostro cliente, ricerchiamo un Regulatory Affairs Specialist da inserire nel team. Il professionista supporterà la registrazione globale di prodotti farmaceutici, garantendo la conformità normativa per i mercati di tutto il mondo.ResponsabilitàDossier e Registrazioni: Sarà responsabile della...


  • roma, Italia Michael Page A tempo pieno

    OverviewAzienda con attività farmaceutica: Per conto di un nostro cliente, ricerchiamo un Regulatory Affairs Specialist da inserire nel team. Il professionista supporterà la registrazione globale di prodotti farmaceutici, garantendo la conformità normativa per i mercati di tutto il mondo.ResponsabilitàDossier e Registrazioni: Sarà responsabile della...


  • Giuliano di Roma, Italia TransPerfect A tempo pieno

    A medical device company in Rome is seeking a Regulatory Affairs Specialist to support CE marking activities and ensure regulatory compliance for medical devices. The ideal candidate will have 3-5 years of experience in Regulatory Affairs, strong knowledge of CE marking regulations, and excellent communication skills in English. This role involves...


  • Roma, Italia Synergie Italia A tempo pieno

    REGULATORY AFFAIRS SPECIALIST In qualità di Regulatory Affairs Specialist, verrai inserita / o nel team dedicato agli Affari Regolatori e supporterai le attività legate alla gestione della documentazione tecnica e regolatoria relativa agli API prodotti dall’azienda. Il ruolo prevede interazioni con le funzioni interne (Qualità, Produzione, Ricerca &...