CMC Regulatory Affairs Consultant: Post-Approval Vaccines/Bio

17 ott - Pistoia
Parexel

Parexel is seeking an Regulatory Affairs Consultant
Scopra di più sui compiti quotidiani, le responsabilità generali e l'esperienza richiesta per questa possibilità 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. xjncmbx

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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