Our client develops technology using predictive analytics and AI algorithms to help clinicians make more accurate and faster treatment decisions. We are partnering with out client to bring on a Director of Regulatory Affairs who will be responsible for driving the Regulatory Strategy and the preparation of regulatory submissions required to market or investigate new or modified medical devices in both domestic and international markets.

The Right Talent: 

Bachelor’s degree required, strongly preferred in the biomedical engineering, biology, chemistry or related science.

Minimum 8 years’ experience in the device/diagnostic industry, preferably in the area of regulatory affairs.

Ability to understand and interpret U.S. and international medical device regulatory requirements.