Rebecca is a Facility Reviewer with CDER’s Office of Pharmaceutical Quality, Office of Process and Facilities, Division of Inspectional Assessment. She has accrued over 12 years of inspectional experience with the FDA, including over 3 years as a District Pre-Approval Manager, 2 years as a Drug Specialist, and a year as a District Drug Program Supervisory Investigator. In this capacity, she attained Level II and Level III Drug Investigator Certification, and was a member of FDA’s Pharmaceutical Inspectorate. Her oversight has included the performance and management of inspectional and reporting related activities associated with the pharmaceutical industry within the Detroit District. She holds a Bachelor of Science and a Master of Science in Biology, and has experience lecturing in both academic and agency forums.