Pieter De Vries
About Pieter De Vries
Pieter De Vries serves as the Director of Quality Europe at AtriCure, Inc., where he has worked since 2019. He has extensive experience in quality assurance and regulatory affairs, having held various roles in the medical technology sector over the past three decades.
Current Role at AtriCure
Currently, Pieter De Vries serves as the Director Quality Europe at AtriCure, Inc., a position he has held since 2019. In this role, he is responsible for overseeing quality management processes within the European operations of the company. He plays a crucial role in establishing the EU Authorized Representative function, ensuring compliance with European regulations. Additionally, he provides strategic support to the parent organization in the United States regarding the EU Medical Device Regulations.
Previous Experience in Quality Assurance and Regulatory Affairs
Prior to his current position, Pieter De Vries worked at MDProject as a Principal Consultant in Quality Assurance and Regulatory Affairs from 2012 to 2019. During his tenure, he contributed to various projects in the Amsterdam Area, Netherlands. Before that, he served as a Project Manager for Certification of Medical Devices at DEKRA Certification B.V. from 2003 to 2012. His experience in these roles has equipped him with extensive knowledge in quality systems and regulatory compliance.
Background in Biomedical Engineering
Pieter De Vries has a solid foundation in biomedical engineering, having worked as a Team Lead in Biomedical Engineering at the Academic Medical Center from 1988 to 1997. This nine-year experience in the Amsterdam Area, Netherlands, allowed him to develop expertise in the intersection of engineering and medical applications. His educational background includes a Bachelor of Engineering in Medical Technology from NHL Hogeschool.
Education and Qualifications
Pieter De Vries earned a Bachelor of Engineering (Ing.) in Medical Technology from NHL Hogeschool. This academic qualification laid the groundwork for his career in the medical device industry, where he has focused on quality management and regulatory affairs. His educational background supports his roles in various organizations, contributing to his understanding of medical technology and compliance standards.