- Prepare and coordinate regulatory submissions for pharmaceutical products to COFEPRIS.
- Support preparation and compilation of dossiers for current product registrations, renewals, variations/modifications, and other applicable regulatory procedures.
- Provide regulatory support to cross-functional teams.
- Handling of deficiency responses of Marketing Authorization Applications
- Communicate with partners for timely information availability
- Ensure timely submission of variation and commercial urgency requests to relevant regulatory authorities
- Maintenance of different project trackers
- Renewals and other applicable lifecycle activities