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Quality Engineer - Medical Device Manufacturer

Streamwood, Illinois Permanent USD80,000 - USD95,000 per year View Job Description
Our client is looking for a Quality Assurance Engineer to ensure their medical devices consistently meet quality, performance, and regulatory standards across both design and manufacturing stages. This role includes responsibility for maintaining quality systems, conducting testing and audits, managing CAPA processes, and working closely with engineering and manufacturing teams.
  • Work on life saving medical devices
  • Join a growing team

About Our Client

Our client has over 40 years of experience as a leader in the design and manufacture of innovative medical devices used in minimally invasive procedures. Their products support a range of specialties-including urology, gastroenterology, laparoscopy, and endoscopy-helping to enhance patient outcomes, improve surgical efficiency, and ensure safety. They are now looking to add a talented Quality Assurance Engineer to their team.

Job Description

  • Establish activities for the development, application and maintenance of quality standards for processes, finished devices, materials, and other products
  • Develop standards and methods for inspection, testing, and evaluation, utilizing knowledge in engineering fields such electrical, and mechanical
  • Develop sampling procedures, forms and instructions for recording, evaluating, and reporting quality and reliability data
  • Develop methods and procedures for disposition of discrepant material and devise methods to assess cost and responsibility
  • Collaborate with Regulatory affairs to meet the requirements of the FDA and Medical Device Directive
  • Manage CAPA program for areas of responsibility



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

  • Bachelor's degree in Engineering
  • 3+ years of experience in manufacturing/quality
  • 2 years of work experience with regulated electro-mechanical medical products in a manufacturing environment
  • Ability to manage multiple, simultaneous projects and deadlines
  • Ability to synthesize and document requirements
  • Excellent written and verbal communication skills
  • Must be able to work independently, in a team environment, and with cross-functional teams
  • Working knowledge of Statistical software package Minitab, InfinityQS, Microsoft Word and Excel
  • Experience in internal auditing of Quality Management Systems
  • Sponsorship is not provided

What's on Offer

  • Compensation up to $95,000 depending on experience
  • 3 weeks of PTO
  • Medical, dental, and vision
  • Short term/long term disability
  • Tuition reimbursement
Contact
Ben Aldrich
Quote job ref
JN-062026-7043068

Job summary

Sector
Engineering & Manufacturing
Sub Sector
Quality, Technical
Industry
Industrial / Manufacturing
Location
Streamwood
Contract Type
Permanent
Consultant name
Ben Aldrich
Job Reference
JN-062026-7043068