Quality Engineer - Medical Device | Great 401(k) Matching!

Itasca, Illinois Permanent USD75,000 - USD90,000 per year View Job Description
Our client specializes in sheet metal fabrication and injection molding for the industrial and medical device sectors, and they're seeking a Quality Engineer to join their expanding quality team. They're looking for a skilled engineer who thrives in a fast-paced environment and brings an outgoing, collaborative personality.
  • Variety of products and customers
  • Excellent benefits package

About Our Client

Our client, a leading sheet metal fabricator and injection molder, also offers welding, powder coating, blanking, and a range of other manufacturing processes for the industrial and medical device industries. They hold ISO 9001 and ISO 14001 certifications and operate out of a spacious, state-of-the-art facility spanning over 160,000 sq. ft., with a team of approximately 200 employees. This is a great opportunity to join a dynamic organization with a diverse product line and customer base, where every day brings new challenges and excitement.

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 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!

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
Contact
Ben Aldrich
Quote job ref
JN-032025-6693590

Job summary

Sector
Engineering & Manufacturing
Sub Sector
Quality, Technical
Industry
Industrial / Manufacturing
Location
Itasca
Contract Type
Permanent
Consultant name
Ben Aldrich
Job Reference
JN-032025-6693590