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R&D Engineer

Job in Salt Lake City, Salt Lake County, Utah, 84193, USA
Listing for: MillenniumSoft Inc
Full Time position
Listed on 2026-08-28
Job specializations:
  • Engineering
    Quality Engineering, Mechanical Engineer, Manufacturing Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 20 - 30 USD Hourly USD 20.00 30.00 HOUR
Job Description & How to Apply Below

Level Of

Experience:

Mid-Level

Position : R&D Engineer

Location :
Salt Lake City, UT

Duration : 12 Months

Total Hours/week : 40.00

pay rate-$20-30/hr

1st

Shift

Client:
Medical Device Company

Job Category:
Engineering

Level Of

Experience:

Mid-Level

Employment Type:
Contract on W2 (Need US Citizens or GC Holders Only)

Hours 8-5 Mon
- Fri

Job Description

  • The preferred candidate should have experience completing technical design analysis including first principles design calculations, stress analysis, FEA, design of experiments, and statistics for medical devices.
  • The preferred candidate will also understand medical device design control, excellent written and oral skills, and leadership abilities.

Duties and responsibilities for this role include but are not limited to the following:

Technical Product Design

  • Drive design and development of product systems, subsystem, and components by understanding design space with design options and trade-offs, managing critical parameters, using design for manufacture principles as well as geometric dimensioning and tolerancing tools.
  • Strong design control experience
  • Developed understanding of DOE and statistical methods.
  • Integrate product systems and subsystems to meet business objectives by addressing customer needs and product requirements under defined cost targets.
  • Identify the best tools and approaches to effectively solve engineering problems to develop/optimize designs by leveraging appropriate mix of first principles / analytical, computational, and experimental methods.
  • Ensure implementation and rigor of product development processes and design control procedures.
  • Support current products in terms of quality, manufacturing, supply continuity and cost improvement.
  • Support execution of technical and/or cross-functional project work.
  • Analyze design solutions using engineering first principles and advanced engineering methods such as FEA
  • Write detailed technical reports based on design verification analysis/testing for design changes and product design activities
  • Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis
  • Develop realistic and actionable design plans.
  • Demonstrate strong accountability for successful completion of designated tasks
  • Develop deliverables schedules and demonstrate accountability for successful completion of tasks/projects and team deliverables
  • Effectively collaborate with laboratory technicians and support staff

Desired Qualifications

  • BS or MS degree in Engineering (Mechanical Engineering, Materials Science & Engineering, Biomedical Engineering, or a closely related engineering degree required)
  • Minimum of 3 years of engineering experience or equivalent is required with a strong preference for least 2-year product development and design experience in medical devices / products
  • Medical device design and development experience related to high-volume manufacturing is strongly preferred.
  • Strong communication skills.
  • Team oriented.
  • Demonstrated ability to utilize statistical tools, computer analysis and engineering fundamentals to support sound engineering judgment. Solidworks, Minitab, and FEA (Abaqus / Fluent) experience is preferred.
  • Developed understanding of DOE and statistical methods.
  • Understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions
  • Experience with contact and non-contact metrology
  • Experience with manufacturing process validation including strategy development, First Article Inspection, Factory Acceptance Testing, and IQ/OQ/PQ’s.
  • Knowledge of disciplined product development processes, regulatory and quality requirements such as 21

    CFR
    820.30
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