Kelly Stanton is an experienced quality assurance professional with over 17 years in the pharmaceutical, biotech, and medical device industries. Currently serving as the Head of Quality Systems Improvement at Corden Pharma, Kelly focuses on enhancing quality systems to support manufacturing operations while ensuring compliance and scalability. Previous roles include Director of Quality at Qualio, where guidance on product development was provided to meet industry requirements, and Senior Quality Assurance Manager at Reven, LLC, overseeing QA for a start-up pharma environment. Kelly's extensive background includes consulting for Endexis Consulting, reestablishing ISO 13485 certification at CHD Bioscience, and managing quality systems at Cochlear. A graduate of Texas A&M University with a Bachelor of Arts in Biology and Chemistry, Kelly has a proven track record in implementing and improving quality systems across various organizational settings.
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