pParexel is seeking an Regulatory Affairs Consultant - 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. /ppYou will support worldwide regulatory activities, manage regulatory information systems, and identify risks to timelines and approvals in a dynamic, global team. /p #J-18808-Ljbffr
📌 CMC Regulatory Affairs Consultant: Post-Approval Vaccines/Bio (Italia)
🏢 Parexel
📍 Italia
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