Sarah Esterquest

Sarah Esterquest is an experienced professional in regulatory affairs and quality assurance, currently serving as the Director of Regulatory Affairs at Cytovale since November 2020, where responsibilities include regulatory strategy, submission management, and product lifecycle management for the IntelliSep test. Previously, Sarah was promoted to Director of Quality Assurance and Regulatory Affairs at Cytovale, successfully leading efforts for the company's first 510(k) submission and managing key regulatory responses. Prior experience includes roles at Takeda, Regeneron Pharmaceuticals, CR Bard, SMC Ltd., and various research positions, offering a comprehensive background in quality engineering, device compliance, and regulatory interactions. Sarah holds a Bachelor's degree in Mechanical Engineering from Rensselaer Polytechnic Institute and has a strong foundation in both engineering and regulatory processes from earlier academic and professional experiences.