Leigh Boutilier

Director, GMP Quality Assurance at Blueprint Medicines

Leigh Boutilier has a diverse work experience spanning over several companies and roles. Leigh started their career as a Programs Coordinator at Maritime Aquarium in Norwalk, CT in 1997. Leigh then moved on to work as a Documentation Specialist II at Alexion Pharmaceuticals from 1998 to 2001. Leigh joined Vitex as a Quality Assurance Specialist II from 2001 to 2003 and later worked as a Quality Assurance Specialist II at Idenix Pharmaceuticals from 2004 to 2006. Leigh then became the Manager of Quality Assurance at Altus Pharmaceuticals from September 2006 to March 2009. From July 2009 to January 2014, they worked at Cubist Pharmaceuticals as a Manager and Senior Manager of GMP Quality Assurance. Leigh briefly worked as a Contractor at Alnara Pharmaceuticals in 2009. From July 2015 to June 2018, Leigh worked at TESARO, Inc. as a Senior Manager of Quality Assurance. Currently, they are employed at Blueprint Medicines as an Associate Director of Quality Operations since July 2018 and recently promoted to Director of GMP Quality Assurance in January 2021.

Leigh Boutilier studied Biology at Western Connecticut State University.

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