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.
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📌 Global Cmc Regulatory Affairs Consultant For Vaccines/Bio (Verona)
🏢 Parexel
📍 Verona
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