Michael Koczocik
About Michael Koczocik
Michael Koczocik is a Regulatory Affairs Specialist at Butterfly Network, Inc. with extensive experience in medical device registration and maintenance.
Current Role at Butterfly Network, Inc.
Michael Koczocik is currently employed as a Regulatory Affairs Specialist at Butterfly Network, Inc. In this role, he is responsible for managing regulatory compliance and ensuring that the company's medical devices meet both domestic and international standards. His extensive experience in the regulatory field allows him to navigate complex regulatory landscapes and contribute significantly to the development and maintenance of the company's product portfolio.
Previous Experience at Defibtech, LLC
Michael Koczocik worked at Defibtech, LLC in various roles over a span of four years. He served as a Senior Regulatory Affairs Specialist from 2018 to 2020 and as a Regulatory Affairs Specialist from 2016 to 2018. During his tenure, he was involved in the regulatory submissions and maintenance of medical devices, contributing to their market approval and compliance with regulatory requirements.
Regulatory Work at Medtronic
From 2013 to 2016, Michael Koczocik was a Regulatory Affairs Specialist at Medtronic. In this capacity, he played a crucial role in regulatory affairs for medical devices, focusing on ensuring that the products met all regulatory standards. His work in this period was integral to the successful approval and market launch of various medical devices.
Experience at the FDA
In 2012, Michael Koczocik worked as a Health Science Project Specialist at the FDA in Silver Spring, MD, for eight months. His role included project management and contributions to regulatory science projects, providing him with valuable insights into the regulatory processes from the perspective of a federal agency.
Educational Background
Michael Koczocik obtained a Master's degree in Regulatory Affairs for Drugs, Biologics, and Medical Devices from Northeastern University, studying from 2011 to 2013. He also holds a Bachelor's degree in Clinical Laboratory Science/Medical Technology/Technologist from the University of Connecticut, where he studied from 2002 to 2006. This educational background has provided him with a strong foundation in both regulatory affairs and clinical laboratory practices.