European Regulatory Affairs Specialist - MA & Lifecycle

Organon in Ireland is seeking a Specialist, Regulatory Affairs to support regulatory activities across Europe, including centralized, MRP, DCP, CP, and national procedures. You will coordinate submissions, maintain registrations, and act as regulatory contact with health authorities.

The role requires 2+ years in pharmaceutical regulatory affairs, fluency in English, and collaboration with Quality, Supply, Medical, and other teams to ensure compliance and timely approvals.