Christopher (Matt) Brown
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Fähigkeiten und Kenntnisse
Werdegang
Berufserfahrung von Christopher (Matt) Brown
- Current 14 years and 7 months, since Nov 2011
VP of Quality and Regulatory Affairs
Remington Medical, Inc.
- 1 year and 8 months, Apr 2010 - Nov 2011
Director of Quality and Regulatory Affairs
Chemence Medical, Inc.
- 3 years and 11 months, Jun 2006 - Apr 2010
Senior Quality Engineer - Medical Devices
Barco, Inc.
• Quality and Regulatory focused, FDA-regulated facility producing Class II medical devices • Developed new QMS for medical division to achieve compliance • Developed process, labeling and quality procedures for repacking line • Lead internal auditor for Title 21 CFR, ISO 13485:2003, ISO 9001:2000, CMDR SOR/98-282 • Six Sigma project lead (yellow belt) • US contact for quality issues in US and Canada • US contact for recalls, 510(k), FMEA, process validation, CAPA, etc. • Quality training
- 3 years and 4 months, Mar 2003 - Jun 2006
Manufacturing Process Engineer
Kimberly-Clark Corp.
• Quality-focused, FDA-regulated facility producing disposable Class II Medical Devices • Department lead of project to implement ISO 9002:1994 and ISO 13488:1996 quality standards and later to upgrade to ISO 13485:2003 standards --Developed document control system adopted facility-wide. --Assisted with FMEA, 510(k), etc. --Validation Review Board --Supervise test lab • Data analysis (DOEs, sampling plans) • Product and Process Improvement • CAPA, Complaint Investigations
Ausbildung von Christopher (Matt) Brown
- 2 years and 5 months, Jan 2008 - May 2010
Regulatory Affairs
University of Georgia
Current GPA: 3.95 National Scholars Honor Society
- 5 years and 5 months, Aug 1993 - Dec 1998
Industrial Engineering
University of Tennessee
Major GPA: 3.78 Overall GPA: 3.42 General Business minor Alpha Pi Mu Industrial Engineering Honor Society
Sprachen
English
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