CMC Module 3 Authoring Specialist for Global Submissions

Importante grupo in Bogotá is seeking a detailed-oriented CMC Analyst to author Module 3 technical documentation for regulatory submissions. The successful candidate will have a strong background in developing content aligned with FDA, EMA, and ICH standards.

This role requires a Bachelor's or Master's degree in a scientific field along with substantial technical authoring experience. Collaboration with various teams is essential for ensuring compliance and quality in documentation.