Senior Quality Engineer | Medical Device Manufacturing

• Handling day-to-day design, supplier, production, and customer quality issues related to production lines
• Resolving non-conformances in the production process by identifying the root cause and implementing solutions
• Assist with internal audits to help the company maintain ISO 13485 compliance
• Lead internal IQ/OQ/PQ process
• Assisting with the application and monitoring of established inspection procedures and methods
• Leveraging data findings to implement improvements in the process
• Preparing documentation for customers and suppliers pertaining to quality standards
• Reviewing manufacturing instructions for completeness, correctness, and comprehension by assembly personnel
• Generating standards for suppliers and internal processes

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.