Vascular Medical Device Design Engineer (Hybrid)

Energy Jobline ZR; Tempe (AZ); Hybrid; USD 55.000 - 83.000; Vollzeit

Zusammenfassung

System One is seeking a Contract Device Design Engineer in Tempe, AZ to design, validate, and bring medical devices to market. The role emphasizes DFMEA, design controls, and cross-functional collaboration in a regulated environment.

The engineer translates user needs into design inputs, develops test fixtures, executes DOE studies, and maintains the Design History File, aligning with production and clinical feedback. Hybrid schedule, Mon–Fri, first shift.

Qualifikationen

• BS Degree in Engineering required.
• 3-5 years experience required.
• Vascular device engineering experience.
• Ability to communicate plans and technical information to team members and managers.
• Experience creating product test fixtures and developing test methods for verification and validation.

Aufgaben

• Research, design, develop, modify, and verify components and systems for medical devices with minimal supervision.
• Translate user needs to design inputs/specifications and produce system-level designs.
• Develop and analyze solutions, prototyping options for proof of concept.
• Apply fundamental and advanced concepts for problem solving.
• Support problem solving, root cause analysis, and evaluate solutions against requirements.
• Develop bench testing methods, conduct measurement system analysis, and develop DOE.
• Conduct studies to support product design and understand customer needs.

Kenntnisse

Vascular device engineering

DFM principles

Regulated environment experience

Problem solving

Ausbildung

Bachelor's degree in Engineering

Tools

DOE methods

Test fixture design

Design controls

Jobbeschreibung

System One is seeking a Contract Device Design Engineer in Tempe, AZ to design, validate, and bring medical devices to market. The role emphasizes DFMEA, design controls, and cross-functional collaboration in a regulated environment.

The engineer translates user needs into design inputs, develops test fixtures, executes DOE studies, and maintains the Design History File, aligning with production and clinical feedback. Hybrid schedule, Mon–Fri, first shift.