Reprise Biomedical is an early commercial stage biologics wound care company focused on bringing unique clinical solutions to the unmet needs of physicians. With our transformational Miro3D wound matrix on the market and new products in development we are ready to begin our growth with an internal regulatory affairs department. We are seeking a knowledgeable, hands-on, Sr. Regulatory Affairs Product Specialist with the ability to independently handle all aspects of Regulatory Affairs for a small but growing medical device company with class I and class II U.S. based products both on the market and in various stages of development. In this role you will: Lead the regulatory strategies for new products by preparing, submitting, and defending 510(k) submissions t