Olivia D.

Olivia D. is an experienced regulatory analyst currently employed at Pearl Pathways since July 2020, focusing on regulatory submissions and quality control. Prior roles include serving as a Regulatory Affairs Associate at Abbott, where strategic plans for product submissions to regulatory agencies were developed, and at Xttrium Laboratories, where regulatory submission guidelines were utilized for post-approval documents. Olivia's experience also encompasses quality assurance at Cardinal Health, coordinating drug stability programs, and clinical laboratory work at PrairieShore Pain Center PC, identifying active pharmaceutical ingredients through extensive analytical testing. Educational background includes a Bachelor of Science in Biological Science from the University of Illinois Chicago, obtained in 2014.