pParexel 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. /ppThe 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 /p #J-18808-Ljbffr
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