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Glenda Marsh

Regional VP, Regulatory Affairs, EMEA & CAN
Johnson & Johnson Medtech, Switzerland

Glenda Marsh brings over 24 years of global experience in regulatory affairs, program management, and operations across the healthcare industry, including medical devices, biotechnology, and consumer health. Since joining Johnson & Johnson in 2001, she has held diverse leadership roles across North America, Latin America, and EMEA.

Glenda has successfully led regulatory programs from concept to implementation and is known for guiding large teams through complex regulatory changes. She played a key role in implementing EU MDR, UKCA, Swiss, and ENVI requirements for J&J MedTech.

Currently, Glenda leads Regulatory Affairs for the EMEA region and Canada, driving innovation and managing a broad portfolio of medical devices. She holds a master’s from Stevens Institute of Technology and a bachelor’s in chemical engineering from the University of São Paulo.

Based in Zug, Switzerland, Glenda continues to shape regulatory strategy and patient access across the region.

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