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Paul M. Kirsch

Vice President, Regulatory Affairs And Quality Assurance at Zynerba Pharma

Paul M. Kirsch has extensive work experience in regulatory affairs. Paul M. is currently the Vice President of Regulatory Affairs and Quality Assurance at Zynerba Pharmaceuticals since January 2020. Prior to that, they served as the Vice President of Regulatory Affairs at Trevena, Inc. from May 2017 to January 2020. From July 2014 to May 2017, they held the position of Vice President of Regulatory Affairs at Iroko Pharmaceuticals, LLC. Before that, they worked as the Executive Director of Regulatory Affairs at Iroko Pharmaceuticals, LLC from May 2013 to June 2014. Paul also has a long tenure at Teva Global Branded Products (formerly Cephalon, Inc.) where they served as the Sr. Director and Group Leader of Regulatory Affairs from August 1993 to April 2012. Paul M. started their career at Wyeth-Ayerst in September 1983 as a Regulatory Affairs Coordinator.

Paul M. Kirsch obtained a Bachelor of Science (B.S.) degree in Biology, General from the University of Scranton between the years 1979 and 1983.

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Timeline

  • Vice President, Regulatory Affairs And Quality Assurance

    January, 2020 - present

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