Product Development Engineer

Midwest Interventional Systems Inc

Maple Grove (MN)

On-site

USD 75,000 - 90,000

Full time

14 days+
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Benefits offered by this job

Health, Dental, and Vision coverage
HSA with employer contribution
401(k) with employer contribution

Job summary

Midwest Interventional Systems Inc in Maple Grove, MN seeks a Product Development Engineer I to drive design transfer, testing, risk management, and documentation for medical devices under QMSR, ISO 13485:2016, and ISO 14971. You will support design transfer activities, develop and validate test methods, and maintain traceability across development stages.

The role requires 0–3 years in medical device design, SolidWorks proficiency, and experience with Minitab.

Qualifications

  • Bachelor’s degree in Mechanical or Biomedical Engineering (or related field).
  • 0–3 years of experience in medical device design under design controls.
  • Working knowledge of 21 CFR 820/QMSR, ISO 13485:2016, and ISO 14971.
  • Proficiency in SolidWorks; experience with GD&T and tolerance stack-ups.
  • Hands-on prototyping, testing, fixture development, and measurement skills.
  • Experience with Minitab for statistics, DOE, and gage R&R.
  • Preferred: Experience with catheter technologies and relevant anatomy.

Responsibilities

  • Support design transfer activities including DFM/DFA input, pilot builds, process development, and required documentation.
  • Develop and validate test methods; design simple fixtures to enable repeatable testing.
  • Maintain requirements traceability and contribute to formal design reviews.
  • Execute verification protocols, analyze data, and generate compliant reports.
  • Perform feasibility studies, product characterization, and risk analysis.
  • Collaborate cross-functionally with Quality, Regulatory, Manufacturing, and suppliers.
  • Participate in customer meetings and present technical updates as needed.
  • Maintain accurate engineering documentation throughout all development phases.

Skills

Hands-on prototyping
Testing
Team collaboration
Documentation

Education

Bachelor’s degree in Mechanical or Biomedical Engineering

Tools

SolidWorks
GD&T
Tolerance stack-ups
Minitab

Job description

EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.

About the Organization We are a dedicated and multidisciplinary group of problem solvers with decades of engineering expertise. As a leader in complex catheter development we have assembled a team of world class engineers that don't shy away from challenges.

Position Product Development Engineer

Description

The Product Development Engineer I supports product development activities from concept through commercialization, executing design controls, testing, risk management, and documentation in compliance with QMSR, ISO 13485:2016, and ISO 14971.

Duties and Responsibilities
  • Support design transfer activities including DFM/DFA input, pilot builds, process development, and required documentation.
  • Develop and validate test methods; design simple fixtures to enable repeatable testing.
  • Maintain requirements traceability and contribute to formal design reviews.
  • Execute verification protocols, analyze data, and generate compliant reports.
  • Perform feasibility studies, product characterization, and risk analysis.
  • Collaborate cross-functionally with Quality, Regulatory, Manufacturing, and suppliers.
  • Participate in customer meetings and present technical updates as needed.
  • Maintain accurate engineering documentation throughout all development phases.
Position Requirements
Qualifications
  • Bachelor’s degree in Mechanical or Biomedical Engineering (or related field).
  • 0–3 years of experience in medical device design under design controls.
  • Working knowledge of 21 CFR 820/QMSR, ISO 13485:2016, and ISO 14971.
  • Proficiency in SolidWorks; experience with GD&T and tolerance stack-ups.
  • Hands-on prototyping, testing, fixture development, and measurement skills.
  • Experience with Minitab for statistics, DOE, and gage R&R.
  • Preferred: Experience with catheter technologies and relevant anatomy.
Compensation & Benefits

Salary Range: $75,000–$90,000

  • Flexible Time Off; 9 Paid Holidays
  • Health, Dental, and Vision coverage
  • Short- & Long-Term Disability options
  • HSA with employer contribution
  • 401(k) with employer contribution

Exempt/Non-Exempt Exempt

Full-Time/Part-Time Full-Time

Open Date 8/26/2026

This position is currently accepting applications.

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