responsibilities (Maxico Market)
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
Preferred candidate profile
2 to 7 Years of experience required in RA
Required experience in Mexico Market.