Sarah Hurley

Sarah Hurley has a diverse work experience spanning over several companies and roles. Sarah started their career at Hallmark Health as an ISA, where they worked from 1997 to 2005. Sarah then joined Therion Biologics as a Compliance Analyst for an undisclosed period. After that, Sarah worked at Biogen Idec as a Microbiologist and later as a Quality Engineer from 2005 to 2011. Sarah then moved to Genzyme and served as a Quality Engineer specializing in change control for a few months in 2011. Sarah then joined Shire as a Senior QA Specialist, followed by a role as a Senior CMC Regulatory Affairs Associate from 2011 to 2013. Sarah later worked at Synageva BioPharma Corp. as a Corporate Quality Assurance Manager from 2013 to 2015. Sarah then joined Biogen, where they worked for a few months as a Business Process Excellence - Process Documentation specialist in 2015. Sarah joined Takeda in 2016 and had several roles, including Manager CMC Regulatory Affairs, Associate Director Global Regulatory Affairs, and Associate Director QMS & Knowledge Management until 2022. From there, they joined Xalud Therapeutics, Inc. as the Director of Regulatory and Quality Compliance for a year. Currently, Sarah is the Director of Quality Operations at Generate:Biomedicines starting in 2023.

Sarah Hurley earned a bachelor's degree in Biotechnology from the University of Massachusetts Lowell, where they studied from 1998 to 2003. Sarah also holds a certification in Lean Six Sigma - Yellow Belt.