Sarah LeBlanc

Sarah LeBlanc has worked in a variety of roles since 1997. Sarah began their career as an ISA at Hallmark Health in 1997. In 2003, they moved to Therion Biologics as a Compliance Analyst. Sarah then worked as a Quality Engineer and Microbiologist at Biogen Idec from 2005-2011. From 2011-2013, they worked at Synageva BioPharma Corp. as a Corporate Quality Assurance Manager. From 2011-2016, they worked at Shire in roles such as Senior CMC Regulatory Affairs Associate and Senior QA Specialist. From 2016-2019, they worked at Takeda as an Associate Director QMS & Knowledge Management and Associate Director Global Regulatory Affairs. Currently, they are the Director of Regulatory and Quality Compliance at Xalud Therapeutics, Inc.

Sarah LeBlanc obtained a Bachelor of Science degree in Biotechnology from the University of Massachusetts Lowell in 2003. Sarah also holds a Lean Six Sigma Yellow Belt certification.