Related skills
data analysis microsoft office project coordination medical devices regulatory documentation📋 Description
- Support regulatory activities for Medical Devices in Colombia.
- Work under supervision from senior Regulatory Affairs staff.
- Manage regulatory docs, systems updates, and project coordination.
- Collect and track documentation for INVIMA submissions.
- Update regulatory systems, databases, and trackers.
- Coordinate regulatory projects with cross-functional teams.
🎯 Requirements
- Bachelor's degree in Life Sciences, Engineering, Pharmacy, or related field.
- Entry-level role; internships or regulated environments a plus.
- Basic understanding of Colombian medical device regulations (Decree 4725 of 2005).
- Proficiency in Microsoft Office tools.
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