28 ott - Genova
Parexel
Parexel is seeking a Senior Regulatory Affairs Associate to lead post-approval CMC activities for biologics and vaccines. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance.
This role offers remote options in several European locations and focuses on variations, renewals, and market expansions, with responsibilities spanning preparation of submissions, risk mitigation, and regulatory risk escalation.
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