Global CMC Regulatory Affairs Consultant for Vaccines/Bio

Parexel is seeking a Regulatory Affairs Consultant - CMC vax/bio (home or office based) in Teramo, Abruzzo, Italy. You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products and collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions. You will manage regulatory...

Parexel is seeking an Regulatory Affairs Consultant - CMC for post-approval activities related to vaccines or biological products. The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely regulatory outcomes. You will support worldwide regulatory activities, manage regulatory information systems,...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe. You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...