Supervisor, Validation @ (December 2018 - May 2020)
Team Lead, Validation Services @ (January 2018 - December 2018)
Senior System Validation Engineer @ (May 2017 - January 2018)
Quality Test Engineer @ (July 2016 - May 2017)
Development Associate III, Analytical Sciences @ (July 2015 - June 2016)
Development Associate II, Analytical Sciences @ (January 2014 - June 2015)
Development Associate I, Analytical Sciences @ (April 2012 - December 2013)
Quality Control Analyst @ 454 Life Sciences (January 2010 - January 2012)
Assistant Laboratory Technician @ (January 2009 - January 2010)
Michael Sessa Education
Quinnipiac University
Master of Science (M.S.) (Cell/Cellular and Molecular Biology)
2015-2017
University of New Haven
BS (Forensic Science and Biology)
2006-2010
Michael Sessa Skills
Biotechnology
Pharmaceutical Industry
Life Sciences
Molecular Biology
Biochemistry
Data Analysis
Real-Time Polymerase Chain Reaction (qPCR)
High-Performance Liquid Chromatography (HPLC)
ELISA
Microbiology
Software Quality Assurance
Validation
Research
Analytical Method Validation
Computerized System Validation (CSV)
Instrument Validation
GMP
Michael Sessa Summary
Michael Sessa, based in New Haven, CT, US, is currently a Sr. QA Auditor, Computer Systems Compliance, Quality Assurance at Boehringer Ingelheim. Michael Sessa brings experience from previous roles at Boehringer Ingelheim and Thermo Fisher Scientific. Michael Sessa holds a 2015 - 2017 Master of Science (M.S.) in Cell/Cellular and Molecular Biology @ Quinnipiac University. With a robust skill set that includes Biotechnology, Pharmaceutical Industry, Life Sciences, Molecular Biology, Biochemistry and more. Michael Sessa has 4 emails and 1 mobile phone numbers on RocketReach.
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