PERSON RESPONSIBLE FOR REGULATORY COMPLIANCE
Descrizione dell'offerta di lavoro
Il PRRC deve possedere competenze comprovate in campo regolatorio e un’adeguata esperienza nel settore dei dispositivi medici.
Di seguito i requisiti necessari.
- Diploma di Laurea in Giurisprudenza, Medicina, Farmacia, Ingegneria o altre discipline scientifiche.
- Almeno un anno di esperienza in attività regolatorie o di gestione della qualità nel settore dei dispositivi medici (o dispositivi medico-diagnostici in vitro per l’IVDR).
Oppure, se non si possiede un titolo di studio specifico, è richiesta un’esperienza di almeno quattro anni in ruoli regolatori o di gestione della qualità nel settore.
Il candidato inserito dovrà assumere la responsabilità della supervisione e controllo della fabbricazione dei dispositivi in termini di.
- conformità al sistema di gestione della qualità - redazione e aggiornamento della documentazione tecnica e della dichiarazione di conformità UE - attività di sorveglianza e vigilanza post commercializzazione, in modo che siano soddisfatti gli obblighi Si offre contratto a tempo determinato, full time, della durata di 6 mesi rinnovabile.
Ral da definire.
Zona di lavoro Roma Flaminio.
Esperienze lavorative.
Regulatory affairs specialist - 12 mesi Titolo di studio.
Laurea Magistrale Disponibilità oraria.
Full Time Patente.
B
Dettagli dell'offerta
- Imprecisato
- Tutta l'Italia
- Imprecisato - Imprecisato
- 04/12/2024
- 04/03/2025
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