Senior Regulatory Strategist, Drug-Device Submissions

Merck in Switzerland seeks a senior regulatory lead for drug-device combination products. You will own the global regulatory strategy from development through approval and lifecycle management, acting as Device Regulatory Lead within a cross-functional team of experts.Fluency in English is required; MSc with 10+ years in regulatory affairs. You will ensure compliant submissions to health authorities worldwide, including EU MDR, ICH guidelines, and build trusted agency relationships. #J-18808-Ljbffr