Quality Engineer - Medical Device Manufacturer

• Plan, coordinate, and execute quality control programs ensuring compliance to ISO13485 and FDA standards
• Investigate and address customer complaints - CAPA
• Assist with preparing and executing internal and external audits
• Handle document and process controls
• Update documentation and data within the QMS
• Create and direct validations (IQ/OQ/PQ)
• Create PPAP documentation
• Other duties as assigned

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.