Overview
Design Quality Engineer III — Medical Device (Hybrid — Maple Grove, MN) Contract
Job Summary : The Design Quality Engineer will support the application of design controls to projects focusing on design changes, material continuity, regulatory and standards compliance, corrective and preventive actions, and improvements for manufacturability and cost reduction. This individual will work with a cross-functional team to ensure safety, quality, and compliance of products. Imaging diagnostic catheter design changes. Working with a team of 5 Design Assurance engineers. Total team of 20.
Responsibilities
- Ownership of design change projects including scoping, assessment, and implementation.
- Develop, update, and maintain Design History File and Design Input / Output documentation.
- Develop, update and maintain risk management files, such as the Hazard Analysis, Task Analysis, and Design FMEA.
- Develop and execute Design Verification, Design Validation, and Usability protocols and reports to meet or exceed internal and external requirements.
- Provide design quality support in the resolution of PIRs, CAPAs, and NCEPs.
- Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
Quality Systems Responsibilities
Build quality into all aspects of work by maintaining compliance with all quality requirements.
Qualifications
Bachelor's degree in an engineering discipline.Experience in design assurance, quality, or related medical device or regulated industry experience.5 - 7 years of experience with BS; 3 - 5 years with MS.Medical device experience preferred; must have worked in a regulated space.Design quality experience; design assurance experience; risk management experience.Good problem-solving ability.Details
Schedule : 08 : 00 AM - 04 : 30 PMWork Setup : Hybrid – Maple Grove, MN; will transition at the end of Oct to Arbor Lakes facility (1.5 miles away).Contract Length : 12 Months (10 / 20 / 2025 - 10 / 20 / 2026)Maple Grove, MN
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