Quality Engineer - Industrial Medical Device | Itasca, IL

• The Quality Engineer is responsible for analyzing reports and returned products, recommending appropriate corrective actions.
• Prepares documentation for inspection and testing procedures.
• Executes PPAP, APQP, Control Plans, and FMEA documentation, with a solid background in Continuous Improvement Processes.
• Gathers information from customers and communicates it internally and to vendors to ensure customer specifications and expectations are met or exceeded.
• Collaborates with various departments and divisions regarding current and future product configurations.
• Facilitates corrective actions and verifies the effectiveness of their implementation.
• Coordinates technical aspects related to product documentation and addresses manufacturing challenges.
• Contributes to the development and maintenance of policies and procedures for configuration management activities.
• Establishes standards and procedures for inspection and quality assurance, as assigned.
• Engages with vendors to resolve quality-related issues, as needed.
• Operates in an open office environment.

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.