10 ott
|
Parexel
|
Firenze
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. xrdztoy
You will support worldwide regulatory activities, manage regulatory information systems, and identify risks to timelines and approvals in a dynamic, global team.
📌 CMC Regulatory Affairs Consultant: Post-Approval Vaccines/Bio (Firenze)
🏢 Parexel
📍 Firenze