Regulatory Affairs Intern – Product Development
4 giorni fa
Un'azienda dinamica nel settore cosmetico cerca un tirocinante in Regulatory Affairs per supportare il team nello sviluppo prodotto. Il candidato ideale ha una laurea in Farmacia o discipline affini e conosce la normativa cosmetica europea. Le principali responsabilità includono la revisione della documentazione tecnica, il controllo della conformità e il monitoraggio delle novità normative. Offriamo un'opportunità di stage di 6 mesi, con affiancamento e possibilità di apprendimento concreto.#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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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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Line Manager
6 giorni fa
Rome, Italia Resourcing Life Science A tempo pienoWhat to ExpectLine management, training of Regulatory Specialist Training of the direct reports in EMEA / FDA requirements Establish and manage regulatory submission timelines for both new and existing products across key global markets Engage with regulatory authorities and distribution partners to support product registrations Conduct global regulatory...
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Line Manager
6 giorni fa
Rome, Italia Resourcing Life Science A tempo pienoWhat to ExpectLine management, training of Regulatory SpecialistTraining of the direct reports in EMEA / FDA requirementsEstablish and manage regulatory submission timelines for both new and existing products across key global marketsEngage with regulatory authorities and distribution partners to support product registrationsConduct global regulatory impact...
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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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Italy Regulatory Affairs Manager
6 giorni fa
Rome, Italia Resourcing Life Science A tempo pienoA leading life sciences company in Italy is seeking a Regulatory Affairs Manager to oversee regulatory submissions and engage with authorities to support product registrations. The ideal candidate must possess at least 8 years of regulatory affairs experience, including 4 years in a managerial role. Strong knowledge of EMEA and FDA requirements is essential....
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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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Senior Regulatory Affairs Specialist
1 settimana fa
Rome, Italia Altro A tempo pienoRegulatory 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,...
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Rome, Italia Altro A tempo pienoRegulatory Affairs Intern Ricerchiamo una risorsa da inserire in stage nel Team di Sviluppo Prodotto nella sede di Milano per il ruolo diAttività previste -Supporto documentale e normativo : raccolta, revisione e archiviazione della documentazione tecnica necessaria al PIF (Product Information File).Verifica delle schede tecniche e delle SDS (Safety Data...