17 oct
|
Parexel
|
Lérida
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.
J-18808-Ljbffr
📌 Regulatory Affairs Consultant, CMC (Lérida)
🏢 Parexel
📍 Lérida