Brian Johnson is an experienced Regulatory Affairs Specialist with a focus on both medical devices and pharmaceuticals. They currently serve as a Sr. Specialist in Regulatory Affairs at Abbott, where they oversee compliance and submission activities. Brian has previously held roles at notable companies such as Pfizer and Cardinal Health, where they led life cycle maintenance and regulatory submissions. Their background includes extensive experience in quality control and analytical chemistry from positions at Morton Grove Pharmaceuticals and Hospira. Brian is actively seeking new opportunities to apply their regulatory expertise.
Location
Chicago, United States
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