pParexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biological and vaccine products. This role involves post-approval regulatory activities, collaboration across manufacturing, QA, QC, and regulatory teams, and support for variations, renewals, and market expansions. Remote options in Europe are offered. /ppThe role emphasizes writing and reviewing CMC documentation, managing regulatory information systems, and mitigating regulatory risks in a cross-functional setting. /p #J-18808-Ljbffr
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