Senior Consultant - EU Regulatory

Job Summary

A company is looking for a Senior Consultant - MedTech Regulatory Sciences.

Key Responsibilities

• Lead the Clinical Operations team and manage project planning and logistics
• Hold regular client meetings and ensure projects stay within scope
• Monitor performance metrics and manage workload allocation among team members

Required Qualifications

• Bachelor's degree in life sciences or a related field; advanced degree preferred
• 10+ years of medical device regulatory, QMS, and management experience
• In-depth knowledge of EU-MDR, IVDR, ISO13485, and associated legislation
• Experience in leading regulatory teams and managing successful submissions
• Strong preference for a German speaker