Director, Regulatory Affairs, Europe
Leads the European Regulatory Affairs team at GE HealthCare, defining regulatory strategy and ensuring compliance with EU MDR and UK MDR for medical devices. Oversees CE and UKCA marking, manages interactions with Notified Bodies and Competent Authorities, and drives regulatory alignment across quality, legal, and product teams. Focuses on strategic planning, postmarket compliance, and industry engagement in a global healthcare technology environment.