pParexel 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 market expansions with a strong emphasis on regulatory documentation and health authority inquiries. Remote options across Europe are available. /p #J-18808-Ljbffr
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