Quality Engineer - Industrial Medical Device | Itasca, IL

Our client is a sheet metal fabricator and injection molder for the industrial and medical device industries, and they're looking for a Quality Engineer to join the growing quality department. My client is looking for a strong engineer, who is comfortable working in a fast-paced environment and has an outgoing personality.

Client Details

Our client, a sheet metal fabricator and injection molder primarily, also does welding, powder coating, blanking, and other manufacturing processes for the industrial and medical device industries. They are ISO 9001 and ISO 14001 certified. They have a large, modern facility that is over 160,000 sq ft and is home to around 200 employees. This is an opportunity to join an organization with a diverse product line and customer base, where no day is the same, offering an exciting work environment.

Description

• 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.

Please apply below, if you're resume looks to fit in with the criteria. From there, Ben Aldrich from Michael Page will reach out in the next 48 hours if deemed a fit!

Profile

• APQP, FMEA, Corrective Action, Control Plan, & Root Cause Analysis Experience
• Understanding of ISO 9001 standard
• Familiarity with ISO 13485 and ISO 14001 is a nice to have
• Ability to communicate with suppliers and customers
• Background in automotive or medical device industries
• Sponsorship not provided

Job Offer

• Salary ranging from $75,000 - $90,000
• Cigna Health Insurance
• Excellent 401(k) matching
• 2 weeks PTO

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.