Paul Stojanovski

Biography

Paul joined Therapure in August of 2017 with over 30 years of Quality and Operations experience in branded, generic and CDMO pharmaceuticals. Prior to joining Therapure, Paul held senior global quality and compliance executive positions at Mylan and Teva. Throughout his career, he has worked closely with manufacturing operations, product development and supply chain to develop partnerships in alignment of quality with regulatory, client and the business to exceed patient needs. His responsibilities, held at multiple sites globally, has been to provide in-depth knowledge and working experience with regulatory agencies that include Health Canada, US FDA, ANVISA, MHRA, EMA, and TGA. Paul is ultimately responsible for ensuring regulatory compliance and overseeing the quality operations related to the development, validation, manufacturing, testing and release of products manufactured by Therapure for its clients. Paul holds a BSc in Biochemistry and Chemistry from the University of Toronto and is a Charter Chemist of Ontario.

Research Interest

manufacturing operations, product development and supply chain to develop partnerships in alignment of quality with regulatory, client and the business to exceed patient needs.