CMC Regulatory Affairs Consultant: Post-Approval Vaccines/Bio

5 ore fa
Bologna, Emilia-Romagna, Italia PAREXEL Tempo pieno

Parexel is seeking an Regulatory Affairs Consultant

Scopra di più sui compiti quotidiani, le responsabilità generali e l'esperienza richiesta per questa opportunità scorrendo subito verso il basso.
- 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. xbvzest

You will support worldwide regulatory activities, manage regulatory information systems, and identify risks to timelines and approvals in a dynamic, global team.


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