23 ott - Prato
Parexel
Parexel 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.
This position supports variations, renewals, and market expansions with a strong emphasis on regulatory documentation and health authority inquiries.
Remote options across Europe are available.
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