Pamela Leister Bershas

Pamela Leister Bershas has extensive experience in quality assurance and scientific roles within the pharmaceutical industry, particularly at GSK from January 2011 to July 2019, where responsibilities included reviewing and releasing materials for clinical and commercial use, leading change control, and conducting analytical testing in compliance with GMP standards. Prior experience includes positions as a staff scientist at DuPont Pharmaceuticals focused on analytical R&D, a stability analyst at McNeil Consumer Healthcare managing stability samples, and a foundational role at Drexel University where Pamela earned a B.S. in chemistry. Analytical expertise encompasses methodologies such as HPLC and SDS-PAGE, supporting various phases of pharmaceutical development and compliance.