SUMMARY Engineer with the experience in a manufacturing environment blended with strong leadership and management qualification. Highly disciplined and self-motivated. Effective communicator both internationally and domestically an energetic team player. Quality experience in analysis of Root Cause, Corrective and Preventive Action, verification/validation, Assembly line/Operation, Current/new Product, quality improvement/ ensure high level of process and product quality. Known as results oriented and have a customer-focus, get-it-done attitude.

Highlights:

• CAPA, Root Cause
• Audit, SCAR,
• FMEA, PFMEA
• Assembly Line
• Complaints
• Risk Management
• Process Improvement
• Design Quality
• ISO13485, iso 14971
• Medical Device
• QSR 21 CFR 820
• Design & Clinical Risk Management