Supplier Quality Engineer - Class II Medical Device

Des Plaines Permanent USD85,000 - USD110,000
  • High Level Quality role within Medical Device Industry
  • Industry Leading Compensation and Benefits Package

About Our Client

Our client is an FDA-approved leading medical device manufacturer with operations and locations across the globe.

Job Description

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.

Description

  • Responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support teams
  • Manage relationships and key metrics for suppliers
  • This individual will identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements
  • It will be the responsibility of this role to lead the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements
  • Work towards resolving quality issues
  • Initiate root cause analysis
  • Recognize areas for continuous improvement
  • Manage process control and monitor CTQ parameters and specifications and will work to implement various product and process improvement methodologies

The Successful Applicant

  • Bachelor of Science degree in engineering (I.e. Mechanical, Electrical, Biomedical, Plastics, or Chemical)
  • 5-8 years of Quality experience in the medical device industry
  • Certification in Six Sigma (Green/Black Belt Preferred)
  • Experience working in a fast paced medical device manufacturing or design facility
  • Strong familiarity with FDA QSR, ISO 13485 regulations
  • Experience with FMEA and Risk Assessment as they pertain to product development
  • Prior experience working with Customers/Suppliers

What's on Offer

  • Competitive Base Salary ($80-110K)
  • Industry Leading Benefits (Health, PTO, 401K Match)
  • Yearly Performance Bonus
  • Growth Opportunities in Several Departments
Contact
Michael Boyd
Quote job ref
1514065

Job summary

Sub Sector
Location
Contract Type
Consultant name
Michael Boyd
Job Reference
1514065