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Quality Engineer
Job in
Maple Grove, Hennepin County, Minnesota, 55311, USA
Listed on 2026-03-04
Listing for:
PACER GROUP
Full Time
position Listed on 2026-03-04
Job specializations:
-
Engineering
Quality Engineering, Manufacturing Engineer
Job Description & How to Apply Below
Quality Engineer
Job Location:
Maple Grove, MN, 55311
Job Duration: 6 Months
Job Summary:
- Drives improvement and corrective action in the quality of components sourced from outside suppliers.
- Provides technical support in the selection of suppliers.
- Develops acceptance criteria for materials.
- Monitors supplier performance to drive supplier corrective action, manufacturing yield issues and field failures.
- Assess potential new suppliers for technical, quality and manufacturing capabilities.
- Provides technical support for the introduction of components from a new supplier.
- Generates and maintains incoming inspection procedures. Trains inspectors to these procedures.
- Develops and/or sources inspection tools and equipment.
- Assists in generating component specifications.
- Generate test protocols, monitor testing, issue qualification test reports and approve components for use in products.
- Provide input to Design Engineering on new component technology and assist in component selection with quality and reliability analysis.
- Analyses incoming material defects. Dispositions and drives corrective action as necessary. Communicates issues to suppliers.
- Reviews new design specifications and provides input from component quality and manufacturability perspective.
- Investigates field failures related to supplier materials. Develop corrective action plan where necessary.
- May supervise inspectors.
- BS degree in engineering or technical field with minimum of 2 years of relevant experience.
- Experience in medical device, automotive, aeronautical, semiconductor, or other regulated industry.
- Project management: ability to influence cross functional global teams spanning Quality, Operations, R&D, and Sourcing.
- Experience in process validation, design controls, risk management, CAPA, SCAR.
- Organized and self-driven.
- Articulate communicator; adept at packaging and appropriately scaling information to the intended audience.
- Ability to rapidly learn and use new software applications (e.g., PLM, ERP).
- Domestic and international travel up to 25%
- 3+ years of medical device engineering experience preferred.
- Medical Device Industry experience
- Problem Solving and Project Management experience
- Leadership experience on a materials or service commodity team.
- Lead auditor of quality systems experience (ISO 13485 or similar).
- ASQ certification (CQE, CBA, SSGB, SSBB) desired
- Requires expanded conceptual and technical and/or functional knowledge in own job function
- Broadens capabilities in applying concepts in job function
- Demonstrates working knowledge of business and industry practices and company processes to accomplish own work
- No supervisory responsibility; accountable for own contributions and meeting objectives
- Uses and exercises judgment to solve problems in straightforward situations and determine appropriate action/solutions.
- Works under general direction from more senior level roles/manager
- Impacts quality of own work and the work of others on the team; works within guidelines and policies
- Explains factual information of limited complexity to others in straightforward situations
- Organizes, presents and explains data/ information, primarily to internal audiences
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