Global Cmc Regulatory Affairs Consultant Vaccines/Bio
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pParexel is seeking a Regulatory Affairs Consultant - CMC vax/bio in Caserta, Italy, offering home or office based work.
You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products within a regulatory team.
/ppYou will collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely delivery.
Fluent English is required, and experience with Veeva Vault is valued.
/p #J-*-Ljbffr
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Regulatory Affairs Consultant
6 mesi fa
Campagna, Campania, Italia Parexel Tempo pienopIn 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, QC,...