Novo Nordisk in Chile seeks a Regulatory Affairs Specialist to own the regulatory portfolio, from registration to modifications, before the ISP. You’ll work hands-on with biotechnological products, including GLP‑1 therapies, while coordinating with integral teams to align local submissions with international strategies.
Your role involves preparing CTD dossiers, keeping platforms current, and managing discontinuations in compliance with Chilean regulations.
📌 Regulatory Affairs Specialist (Santiago)
🏢 Novo Nordisk
📍 Santiago
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