Quality Engineer - Document Control - Medical Device - JN-052022-5600275

Job Description
Summary
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High growth trajectory
Strong progressive culture

About Our Client

Our Client is a medical device manufacturer located in the Northwest suburbs of Chicago. They are looking for a skilled individual to join their Quality team and handle the primary task of Document Control. If you like a diverse product base and want to join a company that is growing quickly, apply now.

Job Description

Oversee the closure of ECRs (Change requests)
Perform training
Oversee the Corrective Actions
Experience in medical a Plus, but needs experience in regulated industry like Aerospace or Automotive
ISO OR AS9100 experience
Administrative skills, be able to work well on the computer, MS OFFICE, good filing skills
Presentation skills
Project Management experience
Will be leading initiatives and validations
Getting machines they need to validate their product

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

Assertive but not aggressive
Someone that has a data-driven mindset
Analyze data, find data and use it to drive decision making, project decisions
Will need to be a coach, mentor - active people management and growth with the team