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 (Las Palmas de Gran Canaria)
🏢 Parexel
📍 Las Palmas de Gran Canaria
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