24 ago
|
Novo Nordisk A/S
|
Región Metropolitana
24 ago
Novo Nordisk A/S
Región Metropolitana
Novo Nordisk A/S in Chile seeks a Regulatory Affairs Specialist to own the regulatory portfolio from registration to modifications, notifications and discontinuations before the ISP. You will work on biotechnological products and GLP-1 therapies, collaborating with general teams to align local submissions with international strategies.
Key activities include leading registrations, managing CTD submissions, ensuring data accuracy on regulatory platforms, and preparing dossiers in CTD format in
📌 Regulatory Affairs Specialist – Biotech (Región Metropolitana)
🏢 Novo Nordisk A/S
📍 Región Metropolitana