Sarah Hyka
About Sarah Hyka
Sarah Hyka is the Senior Manager of Quality Assurance for CAR-T Manufacturing at Bristol Myers Squibb, with over 25 years of experience in quality assurance and regulatory compliance in the pharmaceutical and medical device industries.
Current Position at Bristol Myers Squibb
Sarah Hyka is currently serving as Senior Manager of Quality Assurance for CAR-T Manufacturing at Bristol Myers Squibb. Based in New Jersey, she leads quality assurance initiatives specifically for CAR-T cell therapy manufacturing. Her role involves ensuring the highest standards of quality and compliance within this specialized field, leveraging her extensive experience in the pharmaceutical industry.
Previous Role at Becton Dickinson
Between 2018 and 2021, Sarah Hyka worked as the Senior Manager of Regulatory Compliance at Becton Dickinson in Franklin Lakes, NJ. In this role, she managed regulatory compliance for the company's medical devices. Her responsibilities included overseeing regulatory audits and ensuring that all products met stringent regulatory standards.
Director of Product Safety at FUJIFILM Medical Systems U.S.A., Inc.
From 2010 to 2018, Sarah Hyka served as Director of Product Safety at FUJIFILM Medical Systems U.S.A., Inc. in New Jersey. During her tenure, she was responsible for leading initiatives related to product safety, ensuring that all medical devices met rigorous safety standards. Her role required a deep understanding of regulatory requirements and product safety protocols.
Quality Assurance Experience at Merck & Co.
Sarah Hyka has substantial experience in quality assurance, having held the position of Senior Auditor at Merck & Co. from 2003 to 2010. In this role, she specialized in regulatory audits and quality systems. This experience provided her with a robust foundation in ensuring compliance with various regulatory standards.
Educational Background at William Paterson University of New Jersey
Sarah Hyka earned her Bachelor of Science degree in Biology from William Paterson University of New Jersey, where she studied from 1991 to 1995. Her educational background laid the groundwork for her extensive career in quality assurance and regulatory compliance within the pharmaceutical and medical device industries.