Parexel is seeking a Regulatory Affairs Consultant - CMC vax/bio (home or office based) in Teramo, Abruzzo, Italy. You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products and collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions.
You will manage regulatory information systems, identify risks to timelines, and contribute to efficient regulatory pathways for life-saving therapies.
📌 CMC Regulatory Affairs Consultant (Campo di Ne)
🏢 Parexel
📍 Campo di Ne
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