Director of Quality & Regulatory Affairs (Medical Devices)

A pioneering medical device startup is seeking a Director of Quality and Regulatory Affairs. This role involves building and overseeing quality and regulatory infrastructure, ensuring compliance with FDA and ISO regulations, and leading cross-functional initiatives. The ideal candidate has over 10 years of experience in quality and regulatory affairs in the medical device industry, demonstrating a strong working knowledge of FDA and ISO standards. This is an opportunity to make a significant impact in a rapidly growing organization. #J-18808-Ljbffr