Cindy Yayac

Cindy Yayac has extensive work experience in the pharmaceutical industry. Cindy currently holds the position of Associate Principal Scientist at Organon since May 2021. Prior to that, they worked at Teva Pharmaceuticals as an Associate Director of Regulatory Affairs from April 2019 to May 2021, and as a Senior Manager of Regulatory Affairs from July 2015 to April 2019. Before Teva Pharmaceuticals, they worked at Meda Pharmaceuticals as a Senior Manager of Regulatory Affairs from July 2011 to July 2015. Additionally, they have held roles at MEDA as a Manager of Regulatory Affairs from December 2008 to July 2011, at Alpharma as a Regulatory Associate from August 2007 to December 2008, at MedPointe Pharmaceuticals as a Supervisor of Development Operations from January 2002 to August 2007, at Bristol-Myers Squibb as a Research Scientist II from May 2000 to January 2001, and at Carter-Wallace Inc. as a Stability professional from August 1988 to May 2000.

Cindy Yayac attended The College of New Jersey from 1993 to 1998, where they obtained a Bachelor of Science (B.S.) degree. No specific field of study was provided for their undergraduate degree. Additionally, Cindy Yayac has a certification in Regulatory Affairs (RAC US) from the Regulatory Affairs Professional Society (RAPS), but the month and year of obtaining this certification were not specified.