SUMMARY Nineteen years of experience in various key engineering and leadership positions with knowledge in Engineering, Manufacturing, Operations and Quality Compliance of Class II and Class III Medical Devices. Strong knowledge of Quality Regulations 21 CFR 820, ISO 13485, ISO 14971, GMP, GLP and MDR's with several years of experience in project management, Quality Engineering, lean sigma and leadership supporting multiple plants and multiple sites in multiple geographies.

Highlights:

• Manufacturing
• Management
• Process Improvements
• Product Development
• ISO
• Risk Management
• Compliance
• NCR