Michael Page
Quality Engineer - Industrial Medical Device | Itasca, IL
Michael Page, Itasca, Illinois, United States, 60143
Quality Engineer
Our client, primarily a sheet metal fabricator and injection molder, also offers welding, powder coating, blanking, and other manufacturing services for the industrial and medical device markets. Certified to ISO 9001 and ISO 14001 standards, they operate a state-of-the-art, 160,000+ sq. ft. facility employing about 200 team members. This is a chance to join a company with a diverse product portfolio and customer base, where each day brings new challenges in a dynamic, engaging work environment. Job 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 your 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!
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. The Successful Applicant
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 What's on Offer
Salary ranging from $75,000 - $90,000 Cigna Health Insurance Excellent 401(k) matching 2 weeks PTO
Our client, primarily a sheet metal fabricator and injection molder, also offers welding, powder coating, blanking, and other manufacturing services for the industrial and medical device markets. Certified to ISO 9001 and ISO 14001 standards, they operate a state-of-the-art, 160,000+ sq. ft. facility employing about 200 team members. This is a chance to join a company with a diverse product portfolio and customer base, where each day brings new challenges in a dynamic, engaging work environment. Job 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 your 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!
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. The Successful Applicant
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 What's on Offer
Salary ranging from $75,000 - $90,000 Cigna Health Insurance Excellent 401(k) matching 2 weeks PTO