YOUR CONTRIBUTION
Within our Global Regulatory Affairs department, you will support the implementation of our new DMS (Document Management System) by migrating data files. Together with you, we will ensure our regulatory processes and contribute to the achievement of our corporate goals. We offer you exciting insights into the regulatory processes of an international pharmaceutical company. Your tasks with us include in particular:
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Supporting Regulatory Experts in international submissions
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Support file management in an electronic data management system
- Support update of file naming in excel sheets for migration of products to an electronic data management system
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Support CMC Manager in updating CMC dossiers for variations
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Completing database entries and checking them for completeness