12 ago
|
Apsida Life Science
|
Argentina
12 ago
Apsida Life Science
Argentina
Apsida Life Science seeks a seasoned regulatory leadership expert to drive submission strategies for complex biologics and biosimilars under ANMAT guidelines. You will author and refine CTD dossiers and manage interactions with authorities, ensuring CMC documentation meets local standards.
You will coordinate with general teams to bridge global development with Argentine regulatory expectations, guide clinical pharmacology inputs, and support lifecycle management and vigilance activities as
📌 Senior Regulatory Expert (Argentina)
🏢 Apsida Life Science
📍 Argentina