Regulatory Affairs Lead — COFEPRIS Submissions

Novo Nordisk is seeking a Regulatory Affairs Coordinator based in Ciudad Madero, Mexico. The successful candidate will lead regulatory submissions to COFEPRIS and develop regulatory strategies for innovative treatments. This pivotal role requires a Bachelor's degree in relevant pharmaceutical sciences and 2-10 years of experience in regulatory affairs within a pharmaceutical company. Candidates should possess deep knowledge of Mexican regulations and excellent stakeholder management skills. Join us and impact patient access to life-changing therapies.