Pharma Regulatory Affairs Consultant – CTD/BLA
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Alsinova seeks Regulatory Affairs Consultants to join our Belgium-based team on a regular basis for client projects across pharma and biotech. You will interpret global regulations, author regulatory dossiers, and collaborate with R&D, QA and manufacturing to support new product introductions at client sites.
The role emphasizes CMC experience, scientific writing, and strong communication in English and either French or Dutch.