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William Teags

William Teags

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Founder - Senior Consultant @ Certified ISO 13485 Lead Auditor - Project Manager - Medical Device Quality Systems
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Education

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University of Illinois Chicago

Non-degree curriculum, Music Recording Engineering 1975-01-01 - 1977-01-01
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College of DuPage

, Music Theory and Composition 1975-01-01 - 1977-01-01

Work Experience

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xPackage.Com, LLC

Current

xPackage.Com, LLC

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Abeona Therapeutics

2018-09-01 - 2019-06-01

Abeona Therapeutics

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Quintiles

2014-01-01 - 2018-05-01

Quintiles

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Zimmer Biomet

2009-03-01 - 2017-12-01

Zimmer Biomet

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Loftware

2014-05-01 - 2015-05-01

Loftware

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Pike Research

2009-01-01 - 2012-01-01

Pike Research

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Terumo Blood and Cell Technologies

2007-02-01 - 2008-08-01

Terumo Blood and Cell Technologies

Skills

Presentations Managed Detection and Response (MDR) Analytical Skills Medical Devices Certified Lead Auditor ISO 13485 Quality System Packaging Validation CAPA FDA Quality Systems Corrective and Preventive Action (CAPA) GMP Continuous Improvement Project Management Strategy Business Development Product Development Manufacturing

Summary

A successful and requested, certified lead quality systems auditor with an extensive background in regulated industries from Medical Devices and Bio-pharmaceuticals to Aerospace and Consumer Products. With more than 35 years of experience in Quality Systems, Global Team Leadership, Project Management, Product Design, Development & Manufacturing, Packaging, Labeling and Information Technology, he is an excellent candidate for quality systems auditing. A skilled verbal communicator, he is comfortable leading audit teams through difficult situations while using his writing skills to provide accurate and understandable audit reports. Comfortable performing audits globally, he uses his diverse manufacturing knowledge and communication skills to lead audits to a successful conclusion. As an audit consultant, he can utilize his many years of industry experience to provide guidance on opportunities for improvement that increase regulatory compliance, decrease defect rates and lead to overall corporate improvements.

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