Susie Moynihan Carlson

WORK HISTORY

EDUCATION

ABOUT SUSIE MOYNIHAN CARLSON

As a Regulatory Affairs Specialist at Medline Industries, LP, I work with a team of professionals to ensure the compliance and safety of medical devices in various global markets. I have five years of experience in international regulatory affairs, where I have contributed to the successful registration, approval, and certification of multiple medical devices in various regions. I have also developed and maintained technical documentation, quality systems, and regulatory strategies in accordance with global standards and regulations. I have a strong background in industrial and systems engineering, which enables me to apply analytical and problem-solving skills to complex regulatory challenges. I am passionate about the medical device industry and its potential to improve the lives and health of people around the world. I am driven by the mission of Medline to provide quality products and services that enhance patient care and satisfaction. I am eager to learn from and collaborate with other experts in the field and to bring my diverse perspective and experience to the team.