Parexel is seeking an experienced Regulatory Affairs Consultant to join our team on a client-dedicated project. The role can be office or home based across European locations, focusing on post-approval CMC activities for vaccines or biologics.
You will develop submission strategies, assess change controls, coordinate with manufacturing and QA, and manage regulatory submissions in integral systems. Fluent English and a strong pharma background are required.
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📌 Regulatory Affairs Consultant, CMC (Madrid)
🏢 Parexel
📍 Madrid
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