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David Letteri Location
Dayton, OH, US
David Letteri Work
2018 -now Director of Quality Assurance and Regulatory Affairs @
2017 -2018 Advance Quality Planning Manager @
2015 -2017 QA and QC Director @
2012 -2015 VP, Quality and Regulatory @ NovoSource, Inc.
2010 -2012 Quality Assurance and Regulatory Affairs Manager @
2007 -2010 Quality Director @ RAM Precision Industries/RAM Medical Solutions
2002 -2007 Quality Director @ Leis Medical, Inc.
1999 -2002 Quality Manager @ Heidelberg Web Systems
1997 -1998 Quality Manager @ Sheridan Systems
1987 -1996 Quality Engineer @ Harris Graphics
1984 -1987 Quality Engineer @
David Letteri Education
Rose-Hulman Institute of Technology 1978-1983
Rochester Area High School
David Letteri Skills
Six Sigma
Team Building
Quality System
ISO 13485
Medical Devices
Quality Auditing
Supplier Quality
Quality Management
Continuous Improvement
Quality Assurance
FDA
CAPA
ISO
Orthopedic
Root Cause Analysis
Lean Manufacturing
Leadership
Process Improvement
Manufacturing
GMP
Quality Control
Manufacturing Engineering
DMAIC
SPC
Design for Manufacturing
Regulatory Compliance
Business Process Improvement
ISO Standards
Java
Strategic Planning
u.s. Food and Drug Administration Fda
Marketing
Testing
u.s. Food and Drug Administration
David Letteri Summary
David Letteri, based in Dayton, OH, US, is currently a Director of Quality Assurance and Regulatory Affairs at Aerobiotix, Inc.. David Letteri brings experience from previous roles at Norwood Medical, X-spine Systems, Inc. and NovoSource, Inc.. David Letteri holds a 1978 - 1983 Rose-Hulman Institute of Technology. With a robust skill set that includes Six Sigma, Team Building, Quality System, ISO 13485, Medical Devices and more. David Letteri has 2 emails on RocketReach.
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