Department: Regulatory Affairs Europe - R&D Reference: RAE11002 For the Regulatory Affairs and Quality Assurance department of R&D in Leiderdorp, the Netherlands, we are looking for a Senior Regulatory Affairs Manager with a focus on development. In this role you are responsible for the strategic regulatory support throughout the entire development, scientific advice procedures, PIP submissions as well as preparation, submission and defense of registration files (Marketing Authorization Applications) according to current legislation, in order to obtain and maintain marketing authorizations. Considering the focus on development you will: Participate as a Project Team Member, representing Regu ... City : Leiderdorp
Company : Astellas Pharma
Experience : Senior Fachkraft / Projektleiter
Category : forschende pharmazeutische Industrie
De gebruiker wenst NIET door bedrijven gecontacteerd te worden.
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