Senior Regulatory Affairs Specialist — Remote 1 Day/Week

4 giorni fa


WorkFromHome, Italia ACARPIA Farmaceutici S.r.l. A tempo pieno

Un'azienda farmaceutica innovativa in Lombardia cerca un Regulatory Affairs Senior Specialist per gestire la registrazione di prodotti. Il candidato dovrà preparare documentazione, definire strategie regolatorie e rispondere a quesiti delle autorità. Richiesta laurea in Chimica o Farmacia e almeno 3-5 anni di esperienza nel settore. Offriamo un contratto a tempo indeterminato, welfare aziendale e lavoro agile di un giorno a settimana.#J-18808-Ljbffr



  • WorkFromHome, Italia Resmed A tempo pieno

    A leading medical technology company is seeking an Advanced Regulatory Affairs Specialist located in Italy. The role involves evaluating regulatory requirements, preparing product registrations for the EMEA region, and ensuring compliance with regional regulations. The ideal candidate should hold a Bachelor's degree in Science or Engineering, have early...


  • WorkFromHome, Italia ACARPIA Farmaceutici S.r.l. A tempo pieno

    Regulatory Affairs Senior Specialist – ACARPIA Farmaceutici ACARPIA Farmaceutici è alla ricerca di una figura da inserire nel proprio team come Regulatory Affairs Senior Specialist. Il candidato sarà coinvolto in tutti gli aspetti del processo di registrazione e mantenimento dell’autorizzazione all’immissione in commercio (AIC) tramite rinnovi,...


  • WorkFromHome, Italia ResMed Inc A tempo pieno

    A leading medical technology company is seeking an Advanced Regulatory Affairs Specialist in Rome, Italy. You will be responsible for regulatory activities related to product registrations and compliance across EMEA. The ideal candidate has a Bachelor’s degree in Science or Engineering, at least 5 years of experience in regulatory affairs, and excellent...


  • WorkFromHome, Italia Resmed A tempo pieno

    Advanced Regulatory Affairs Specialist Join to apply for the Advanced Regulatory Affairs Specialist role at ResMed, located in Italy, GB, or Sweden. Overview As part of the EMEA Regulatory Affairs team, you will participate in all regulatory activities related to the import and distribution of ResMed products in the EMEA region, from product registrations to...


  • WorkFromHome, Italia Resmed A tempo pieno

    Advanced Regulatory Affairs Specialist Join to apply for the Advanced Regulatory Affairs Specialist role at ResMed, located in Italy, GB, or Sweden. Overview As part of the EMEA Regulatory Affairs team, you will participate in all regulatory activities related to the import and distribution of ResMed products in the EMEA region, from product registrations to...


  • WorkFromHome, Italia ResMed Inc A tempo pieno

    A leading global healthcare company is seeking an Advanced Regulatory Affairs Specialist in Vimercate, Italy. In this role, you will participate in regulatory activities tied to the import and distribution of medical devices across the EMEA region. The ideal candidate has a Bachelor's Degree in Science or Engineering and at least 5 years of relevant...


  • WorkFromHome, Italia ACARPIA Farmaceutici S.r.l. A tempo pieno

    ACARPIA Farmaceutici è alla ricerca di una figura da inserire nel proprio team come Regulatory Affairs Senior Specialist. Il candidato, sarà coinvolto in tutti gli aspetti del processo di registrazione e mantenimento dell’autorizzazione all’immissione in commercio (AIC) tramite rinnovi, variazioni e/o adeguamento ai requisiti normativi sia in Italia...


  • WorkFromHome, 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...


  • WorkFromHome, 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...


  • WorkFromHome, Italia Neopharmed Gentili S.P.A. A tempo pieno

    Neopharmed Gentili Spa , azienda farmaceutica italiana, specializzata nella commercializzazione di soluzioni ad alto valore terapeutico ed importante player nel mercato farmaceutico nazionale ed in fase espansiva a livello internazionale è alla ricerca di un / una Regulatory Affairs Specialist. Descrizione del ruolo Il / la candidato / a riporterà ad un /...