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Mary Rose, RAC, currently serves as the Director of Regulatory Affairs at Penumbra, Inc. since August 2014, where responsibilities include managing the Regulatory group and guiding US and International regulatory strategies. Prior experience includes a role as Sr. Manager of Regulatory Affairs at Medtronic Spine & Biologics, where oversight involved reviewing promotional content for implantable surgical devices. At a medical device startup, Mary Rose built the Regulatory Department's infrastructure and developed standard operating procedures. Additional experience spans positions at Abbott Diabetes Care and Guidant Corp., contributing to regulatory affairs for various medical technologies. Mary Rose holds a Bachelor of Science degree in Business from the University of Wisconsin-Stout.