Global CMC Regulatory Affairs Consultant for Vaccines/Bio

4 giorni fa

Ne, Liguria, Italia Parexel Tempo pieno

Parexel seeks a Regulatory Affairs Consultant - CMC vax/bio to 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 role emphasizes collaboration across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions.