Jeanette Keating

Jeanette Keating is a seasoned professional in the medical device and regulatory affairs sectors, currently serving as a Principal Scientist in Device Regulatory at Merck since September 2019. With extensive experience leading quality assurance teams and integrating regulatory compliance across medical device and combination product development, Jeanette has held significant roles at Regeneron Pharmaceuticals, CR Bard, and Zimmer Biomet, among others. Jeanette's background encompasses quality risk management, cross-functional team leadership, and the successful implementation of quality systems and processes. Educational qualifications include a Master’s degree in Biomedical Engineering from Rutgers University and a Bachelor’s degree in Mechanical Engineering from Worcester Polytechnic Institute.