Rhonda Russell is a seasoned professional in quality systems and regulatory affairs with extensive experience in the medical device and pharmaceutical industries. Currently serving as a Sr. Staff Quality Systems Analyst at Stryker since April 2009, Rhonda leads regulatory tracks and consolidates device data for submission to GUDID. Prior to this role, Rhonda worked as a Sr. Staff Regulatory Affairs Analyst at Stryker and as a CQT Consultant at Maetrics, LLC, providing project management and auditing services. Rhonda's previous experience includes positions at Roche Diagnostics, Boston Scientific, Eli Lilly and Company, Dow AgroSciences, and Simon Property Group, where Rhonda focused on compliance, quality management systems, and operational efficiencies. Rhonda holds a Master’s degree in Information and Communication Sciences from Ball State University and a Bachelor’s degree in English (technical writing) from Oakland University.
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