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 general systems. Fluent English and a strong pharma background are required. #J-18808-Ljbffr