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Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biologics and vaccines. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. The role supports variations, renewals, market expansions, and annual reports, with remote options across Europe. You will manage regulatory information systems and prepare documentation for registrations, all while #J-18808-Ljbffr
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