YOUR CONTRIBUTION
Within our Global Regulatory Affairs department, you will support us to prepare our datafiles regarding the implementation to our document management system. 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