16 ott
|
Parexel
|
Campo di Ne
16 ott
Parexel
Campo di Ne
Parexel 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.
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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📌 CMC Regulatory Affairs Consultant: Post-Approval Vaccines/Bio (Campo di Ne)
🏢 Parexel
📍 Campo di Ne