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Diana Rivera has extensive experience in the medical device and combination product sectors, having held significant roles in regulatory affairs and quality assurance at leading companies such as AbbVie and Abbott Laboratories. Currently serving as a Manager in Regulatory Affairs CMC for Medical Devices and Combination Products at AbbVie, Diana previously occupied positions including Senior Quality Assurance Manager and Project Manager at Abbott Laboratories, as well as Quality Assurance roles at Abbott Diagnostics. Diana holds a Master of Science degree in Biochemistry from Chicago Medical School, completed between 1995 and 1999.