CMC Regulatory Affairs Consultant: Post-Approval Vaccines/Bio
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- 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
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Regulatory Affairs Consultant
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Toscana, Toscana, Italia Parexel Tempo pienopIn this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...
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Senior Regulatory Affairs, CMC
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Toscana, Toscana, Italia Parexel Tempo pienopParexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biologics and vaccines. The role involves post-approval regulatory activities, worldwide submissions, and close collaboration with manufacturing, QA, QC, and regulatory teams to drive submission strategies and risk mitigation. /ppThis position supports variations, renewals, and...