Descrizione dell'offerta
Sobi - Swedish Orphan Biovitrum AB (publ) in Milan, Italy, seeks a Regulatory Affairs Specialist to provide regulatory and operational support across lifecycle activities. You will work with internal departments and external stakeholders to ensure regulatory compliance of medicinal products and medical devices where applicable.
The role reports to the RA, QA & PV Associate Director and involves local lifecycle management, regulatory submissions, and ongoing compliance activities.
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Candidatura e Ritorno (in fondo)
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