Associate Director, Compliance and Quality Systems @ (April 2022 - December 2025)
Senior Process Engineer - Clinical Supply Operations, Parenteral Manufacturing @ (May 2021 - April 2022)
Process Engineer - Clinical Supply Operations, Parenteral Manufacturing @ (June 2017 - May 2021)
Specialist, Engineering - Technical Operations and Validation @ (June 2012 - May 2017)
Graduate Biodiesel Synthesis Research @ (March 2011 - June 2012)
Biomaterials Engineering Co-op @ (September 2010 - March 2011)
Pharmaceutical Packaging Technology and Development Co-op @ (September 2009 - March 2010)
Laboratory Assistant @ (September 2008 - March 2009)
Eric Lister Education
Drexel University
Bachelor of Science (BS)/Master of Science (MS) (Chemical Engineering)
2007-2012
Eric Lister Skills
Laboratory
Linux
Experimentation
Aspen Plus
Root Cause Analysis
GMP
Biomaterials
Chemical Engineering
Data Validation
Data Analysis
Finance
Validation
Process Improvement
Visio
Materials
Engineering
Quality Assurance
SAS
Operations
Visual Basic
Testing
Administration
Aspen HYSYS
Teamwork
Product Development
Project Management
Research
Biochemistry
Technical Operations
Analysis
Process Simulation
Eric Lister Summary
Eric Lister, based in East Brunswick, NJ, US, is currently a Associate Director, Validation Quality at Bristol Myers Squibb. Eric Lister brings experience from previous roles at Bristol Myers Squibb and Merck. Eric Lister holds a 2007 - 2012 Bachelor of Science (BS)/Master of Science (MS) in Chemical Engineering @ Drexel University. With a robust skill set that includes Laboratory, Linux, Experimentation, Aspen Plus, Root Cause Analysis and more. Eric Lister has 1 emails and 1 mobile phone numbers on RocketReach.
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