Serves as the Regulatory Affairs lead on cross functional MDR project teams Ensures compliance with EU Medical Device Regulations (MDR) and EU guidance throughout the project. Actively participates in EU MDR project teams by attending meetings, collaborating with the project manager and cross functional team members, and communicating regulatory requirements and guidance

Work on life cycle management product test assignments. Experience in testing of mechanical, electrical, and electromechanical products. Contribute to test data analysis as needed. Collaborate with test technician team and engineering in achieving project goal. Be a part of root cause investigation analysis as needed EXPERIENCE Minimum of three years of experience in test