Design Engineer I, Medical Devices & Catheters

Stereotaxis, Inc.

Minneapolis, Northern (MN, KY)

Hybrid

USD 65,000 - 85,000

Full time

14 days+
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Job summary

Stereotaxis, Inc. in Minneapolis, MN is seeking a Design Engineer I to join the Map-iT facility in Rogers to guide cross-functional teams in compliant development, manufacturing, and sales support for medical devices.

The role emphasizes verification/validation activities, process development, supplier coordination, and documentation, with a focus on catheter products and accessories. Bachelor’s degree and 2–3 years in a related field are required.

Qualifications

  • Bachelor's Degree or Technical Degree in Mechanical Engineering or related field (highly preferred).
  • 2–3 years’ experience in a Medical Device manufacturing environment preferred.
  • Experience/knowledge with process validation.
  • Must possess good project management skills and initiative in taking on and completing projects.
  • Must possess good verbal and written communication skills.

Responsibilities

  • Develops and implements product and process development plans including verification and validation activities to achieve company objectives for products and services.
  • Helps develop and manage new product development and operational projects for the company.
  • Direct and manage relationships with suppliers to ensure objectives are met.
  • Develops requirements and executes equipment installation and qualification plans in collaboration with operations and quality personnel.
  • Responsible for product design, development and production of catheters and accessories.
  • Assists other departments within the organization to prepare manuals and technical publications.
  • Other responsibilities as assigned.

Skills

Project management
Verbal and written communication

Education

Bachelor's Degree in Mechanical Engineering

Job description

Stereotaxis, Inc. in Minneapolis, MN is seeking a Design Engineer I to join the Map-iT facility in Rogers to guide cross-functional teams in compliant development, manufacturing, and sales support for medical devices.

The role emphasizes verification/validation activities, process development, supplier coordination, and documentation, with a focus on catheter products and accessories. Bachelor’s degree and 2–3 years in a related field are required.

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