Michelle Lott
Industry Representative, Device Good Manufacturing Practices Advisory Committee (DGMPAC) at FDA | Greater Tucson Area
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Regulatory Strategist, Principal and Founder at Lean RAQA, LLC in January 2010 to Present
Industry Representative, Device Good Manufacturing Practices Advisory Committee (DGMPAC) at FDA in April 2016 to May 2019
Executive Advisor, Regulatory Strategy at Cognition Corporation in June 2014 to June 2015
RA/QA Director at Xeridiem (formerly MRI Medical) in January 2012 to May 2014
Regulatory Director at Westmed Inc in January 2008 to May 2011
Internal Auditor at Baxter Health Care in January 2005 to January 2008
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Northwestern University - Kellogg School of Management, RAPS Executive Development Program, January 2013
Troy State University, B.S., January 1996 to January 2000
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Due Diligence
Biotechnology
Regulatory Compliance
Audit Management
Risk Management
Regulatory Strategy Development
Medical Devices
ISO 13485
FDA
Quality Systems Design
ISO 14971
Quality System
Regulatory Affairs
Cross-functional Team Leadership
Commercialization
Product Development
Regulatory Requirements
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Discover more about FDAWhat is Michelle Lott email address?
Email Michelle Lott at [email protected], [email protected] and [email protected]. This email is the most updated Michelle Lott's email found in 2026.
What is Michelle Lott phone number?
Michelle Lott phone number is +1.5202759838 and +1.6019557847.
How to contact Michelle Lott?
To contact Michelle Lott send an email to [email protected], [email protected] or [email protected]. If you want to call Michelle Lott try calling on +1.5202759838 and +1.6019557847.
What company does Michelle Lott work for?
Michelle Lott works for FDA
What is Michelle Lott's role at FDA?
Michelle Lott is Industry Representative, Device Good Manufacturing Practices Advisory Committee (DGMPAC)
What industry does Michelle Lott work in?
Michelle Lott works in the Medical Device industry.
Michelle Lott Email Addresses
Michelle Lott Phone Numbers
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