Personal Information
Organización/Lugar de trabajo
Greater Chicago Area United States
Ocupación
Quality Engineer II at Lake Region Medical
Sector
Medical / Health Care / Pharmaceuticals
Acerca de
• Seven years of work experience in implementing quality requirements in cGMP and FDA regulated industry.
• Six years of product knowledge related to medical devices and ISO 9000, 13485 and 14971 standards.
• Certified Quality Engineer (CQE) with proven ability in design controls, risk assessments, gage R&R, GD&T, SPC and DOE.
• Certified Quality Auditor (CQA) to have co-led and supported FDA, Saudi Arabia, TUV, EU, Client, Supplier and Internal audits.
• Excellent written, communication, interpersonal and problem resolution skills.
• Work attitude that exhibits strong attention to detail, result and decision making.
• Possess strong skills in Microsoft Office, Lean Six Sigma (DMA...
Presentaciones
(1)Personal Information
Organización/Lugar de trabajo
Greater Chicago Area United States
Ocupación
Quality Engineer II at Lake Region Medical
Sector
Medical / Health Care / Pharmaceuticals
Acerca de
• Seven years of work experience in implementing quality requirements in cGMP and FDA regulated industry.
• Six years of product knowledge related to medical devices and ISO 9000, 13485 and 14971 standards.
• Certified Quality Engineer (CQE) with proven ability in design controls, risk assessments, gage R&R, GD&T, SPC and DOE.
• Certified Quality Auditor (CQA) to have co-led and supported FDA, Saudi Arabia, TUV, EU, Client, Supplier and Internal audits.
• Excellent written, communication, interpersonal and problem resolution skills.
• Work attitude that exhibits strong attention to detail, result and decision making.
• Possess strong skills in Microsoft Office, Lean Six Sigma (DMA...