Merck Gruppe - MSD Sharp & Dohme in Mexico City seeks an experienced Regulatory Affairs Manager (Senior Specialist) to lead regulatory submissions, lifecycle management, and compliance for oncology products. You will coordinate with COFEPRIS and cross-functional teams to secure timely MA approvals and maintain product registrations.
The role demands extensive knowledge of local regulations, strong English skills, and the ability to drive regulatory strategies in a dynamic environment.
📌 Oncology Regulatory Affairs Lead – COFEPRIS Expert (Ciudad de México)
🏢 Merck Gruppe - Msd Sharp & Dohme
📍 Ciudad de México
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