Global Regulatory Lead, Drug-Device Combos

pMerck KGaA is seeking a senior Regulatory Lead to own the global regulatory strategy for drug-device combination products, guiding submissions from early development through approval and lifecycle management. You will work with CMC, device engineering and quality teams to ensure compliant, timely, and scientifically credible submissions worldwide. /ppThe role requires extensive regulatory affairs experience, strong US/EU/international submission expertise, and proven collaboration with regulatory /p #J-18808-Ljbffr