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Glenda Marsh

Sr. Director, EMEA Regulatory Afairs
Johnson & Johnson Medtech, Switzerland

Glenda Marsh is a corporate executive with over 20 years of global experience in regulatory affairs, program management and operations across the health-care industry, including medical devices, biotech and consumer products. She has extensive experience in leading large organizations through major regulation changes, with a focus on building organizational capabilities and ensuring continued and timely patient access to life-saving medical technology.

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

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