Glenda Marsh

Glenda Marsh is an accomplished, proactive, and versatile corporate professional with over 20 years of global experience in regulatory affairs, program management and operations across the health-care industry, including bio-pharm, medical devices and consumer products.

Since joining Johnson & Johnson in 2001, she has held positions of local, regional and global responsibility and covered different J&J sectors, companies, functions and regions (Latin America, North America and EMEA). She has led regulatory programs from concept to approval and implementation spanning the entire medical device product lifecycle.

Glenda has extensive experience in leading large organizations through major regulation changes, with a focus on ensuring short and long-term continued and timely patient access to life-saving medical technology. Since 2016, Glenda has played a strategic leadership role in the preparation for and implementation of the EU MDR (Medical Device Regulation), and more recently, UKCA and Swiss MedDO requirements, for all J&J MedTech companies.

Currently, Glenda leads Regulatory Affairs in EU markets ensuring successful execution of the global innovation agenda as well as life cycle maintenance of an extensive medical devices portfolio.

Glenda has a master’s degree in chemical engineering from Stevens Institute of Technology and a bachelor’s degree in Chemical Engineering from the Polytechnic School of the University of Sao Paulo.