Pertrice Auguste Wethey
leadership in manufacturing project management and quality@ Confidential
Victor, New York, United States
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Pertrice Auguste Wethey is a highly experienced Validation Manager with over 25 years of work experience in process and equipment validation within the medical device industry. He is responsible for implementing a risk-based validation program and ensuring compliance with FDA 21 CFR 820, ISO 13485, and MDSAP. Pertrice is detail-oriented and has successfully executed multiple projects simultaneously. With over 15 years of experience in validations in a regulated environment, including 5 years in medical devices, he has a strong track record in lean manufacturing, FMEA, continuous improvement, and engineering.
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Emails and Phone Numbers

@lsisolutions.com
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About

A Validation Manager with experience in process and equipment validation within the medical device industry. Responsible for the implementation of a risk based validation program compliant with FDA 21 CFR 820, ISO 13485 and MDSAP. I am a detail oriented individual with the ability to successfully execute multiple projects simultaneously. Over 15 years of experience with validations in a regulated environment; including 5 years in medical devices.

Work Experience

Silicon Valley, California, US
9771
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Pertrice Auguste Wethey's Professional Milestones

  • Engineer (1998-01-01~2011-08-01): Developing innovative solutions to optimize production processes and drive efficiency, resulting in increased productivity and cost savings.
  • Continuous Improvement Engineer (2011-11-01~2013-11-01): Driving continuous improvements by implementing innovative solutions and optimizing processes.
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Education

Western Michigan University
Western Michigan University

Materials Science,

Engineering,

Master Of Science,

Masters

2002-2003
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