Cmc Regulatory Affairs Consultant: Post-Approval Vaccines/Bio

03 ott - Uri
Parexel

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