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R&D Development Engineer - Mechanical

Job in West Valley City, Salt Lake County, Utah, 84119, USA
Listing for: Ottobock
Full Time position
Listed on 2026-02-18
Job specializations:
  • Engineering
    Biomedical Engineer, Product Engineer, Quality Engineering, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Summary Statement

For more than a century Ottobock has pursued the mission of helping people living with limb loss or mobility challenges regain or maintain their freedom of movement. We do this through the development of leading prosthetic, orthotic and wheelchair innovation and an unwavering commitment to delivering superior patient care experiences. As a growing healthcare company, we continue to invest in both our people and new service offerings.

With more than 10,000 employees worldwide and 1,100 across North America, we are dedicated to advancing the O&P industry and improving the lives of the people serviced by it.

We have an opening for a Product Development Engineer position within our Research and Development team in our Salt Lake City, Utah location.

If you would like to be part of a passionate, hard-working, engineering team that develops products which make a difference in human mobility, then this is an opportunity for you.

The ideal candidate for this position is an experienced and motivated R&D Engineer proficient in both product development and the ongoing support of in-market products.

Duties & Responsibilities
  • Provide technical leadership in a cross-functional environment with manufacturing, quality, regulatory, supply chain, and external partners
  • Technical oversight across design, analysis, testing, and manufacturing activities
  • Oversee iterative design, test fixture development, bench testing, and failure analysis to meet stakeholder and end-user requirements
  • Optimization of product cost / function / features including material selection and analysis.
  • Identification and reduction of product/project risks.
  • Product refinement and design changes for existing products.
  • Provide technical guidance throughout the planning and execution of verification and validation testing
  • Documentation to applicable Medical Device standards.
  • Collaborate with key local/global stakeholders on topics such as product and manufacturability requirements
  • Remain current with technical advances through education, training, and technical research.
  • Other duties as assigned.
  • Some regional or international travel may be required (
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