Senior Research And Development Engineer

ACE Partners

Minnesota

On-site

USD 80,000 - 100,000

Full time

14 days+

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Job summary

A growing, innovation-driven medical device company is seeking a Product Development Engineer to join their R&D team in Minnesota. The role involves leading product development from concept to commercialization, designing minimally invasive medical devices, and collaborating with cross-functional teams. Candidates should hold a Bachelor's or Master’s degree in a related field and have 3–7 years of experience in medical device development. Strong CAD skills and knowledge of design controls are essential.

Qualifications

  • 3–7 years of experience in medical device product development.
  • Experience with minimally invasive or catheter-based technologies.
  • Understanding of design controls and regulated environments (FDA, ISO 13485).

Responsibilities

  • Support and lead product development activities from concept through to commercialization.
  • Design and develop minimally invasive / catheter-based medical devices.
  • Build and refine prototypes, test fixtures, and engineering models.

Skills

Medical device product development
Prototyping
CAD tools (e.g., SolidWorks, NX)
Statistical analysis
Cross-functional collaboration

Education

Bachelor's or Master’s degree in Mechanical Engineering, Biomedical Engineering, or related field

Tools

SolidWorks
NX

Job description

We are working with a growing, innovation-driven medical device company seeking a Product Development Engineer to join their R&D team.

This role offers the opportunity to work on next-generation, minimally invasive technologies, contributing across the full product lifecycle in a collaborative and fast-paced environment.

What You’ll Be Doing
  • Support and lead product development activities from concept through to commercialization
  • Design and develop minimally invasive / catheter-based medical devices
  • Build and refine prototypes, test fixtures, and engineering models
  • Collaborate cross-functionally with R&D, Quality, Regulatory, and Manufacturing teams
  • Develop and maintain design documentation (DHF, protocols, reports)
  • Apply DOE and statistical methods to optimize product performance
  • Support risk management activities (FMEA, hazard analysis)
  • Work with suppliers and partners on component and process development
  • Contribute to continuous improvement initiatives across products and processes
What We’re Looking For
  • Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, or related field
  • 3–7 years of experience in medical device product development
  • Experience with minimally invasive or catheter-based technologies
  • Understanding of design controls and regulated environments (FDA, ISO 13485)
  • Hands‑on experience with prototyping, testing, and iteration
  • Familiarity with DOE, statistical analysis, and problem‑solving methodologies
  • Experience with CAD tools (e.g., SolidWorks, NX, or similar)
  • Strong communication skills and ability to work cross‑functionally
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