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Ryan Lessard Location
Boston, MA, US
Ryan Lessard Work
Director, GMP QA Development @ (April 2024 - Present)
Associate Director, GMP QA @ (October 2021 - April 2024)
Senior Manager, GMP QA @ (April 2021 - October 2021)
Senior Manager, GMP QA @ (October 2019 - April 2021)
Quality Assurance Manager @ (July 2017 - October 2019)
QA Specialist II @ (October 2016 - July 2017)
Compliance Specialist @ Cerulean Pharma Inc. (January 2016 - October 2016)
Senior Associate, Quality Assurance @ Cerulean Pharma Inc. (September 2014 - January 2016)
Senior Quality Control Analyst @ (March 2014 - August 2014)
Quality Control Analyst II @ (March 2012 - March 2014)
Quality Control Analyst I @ (June 2010 - March 2012)
Ryan Lessard Education
University of Vermont
BS (Chemistry)
2006-2010
Ryan Lessard Skills
Quality Control
GMP
Wet Chemistry
Empower
TrackWise
GLP
Assay Validation
Method Transfers
cGMP practices
Deviation Management
Method Transfer
DCR
Sop
Assay Development
Assay Troubleshooting
Corrective and Preventive Action (CAPA)
Risk Management
Change Control
CMO management
Quality Auditing
internal auditing
Batch Records
HPLC
cGMP
Biotechnology Industry
Biotechnology
IOT
Engineering
Software
Corrective and Preventive Action Capa
QC
Compliance
Sds Page
Chemstation
Corrective and Preventive Action
Ryan Lessard Summary
Ryan Lessard, based in Boston, MA, US, is currently a Director, GMP QA Development at Syndax Pharmaceuticals. Ryan Lessard brings experience from previous roles at Blueprint Medicines, Servier Pharmaceuticals, Agios Pharmaceuticals and Wave Life Sciences. Ryan Lessard holds a 2006 - 2010 BS in Chemistry @ University of Vermont. With a robust skill set that includes Quality Control, GMP, Wet Chemistry, Empower, TrackWise and more. Ryan Lessard has 2 emails on RocketReach.
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