Regulatory Affairs Consultant, CMC (Vax/Bio) - Remote
Job Description & Overview
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 global systems. Fluent English and a strong pharma background are required.
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Key Details
- Date Posted: 23 Oct 2026
- Location: murcia
- Employment Type: Permanent
- Category: General
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Parexel
Verified Transport EmployerVerified transport and logistics firm operating commercial fleets across the UK network.
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