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R&D Engineer

Job in Franklin Lakes, Bergen County, New Jersey, 07417, USA
Listing for: MillenniumSoft Inc
Full Time position
Listed on 2026-06-13
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering, Medical Device Industry, Product Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Position

R&D Engineer

Location

Franklin Lakes, NJ

Contract Duration

12+ Months contract

Hours & Shift

40.00 hours/week; 1st Shift

Client

Medical Device Company

Employment Type

Contract on W2 (US Citizens or GC Holders Only)

Eligibility

No H1b’s

Job Summary

The individual in this position will have understanding and exposure to a wide application of technical principles, theories, and concepts. He/She provides solutions that are imaginative, thorough, and practical to a wide range of complex problems. Also, the individual will be available in the testing lab at Franklin Lakes.

Responsibilities
  • Provide solid technical skill and engineering support for design and development activities for new and existing products.
  • Support current products in terms of quality, manufacturing, supply continuity, and cost improvement.
  • Participate in executing technical and/or cross-functional project work.
  • Contribute to a culture of innovation by proactively generating novel concepts for new products and enhancements to current product performance.
  • Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies.
  • Translate customer needs into engineering requirements and specific product, packaging, and process specifications.
  • Engineer robust and manufacturable products through strong understanding and application of engineering fundamentals.
  • Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis.
  • Author detailed technical reports based on design verification analysis/testing for design changes and product design activities.
  • Ensure compliance with client quality policies, procedures, and practices as well as with all local, state, federal and BD safety regulations, policies, and procedures.
Qualifications
  • BS degree in engineering (Mechanical or Biomedical Engineering preferred).
  • 2-4 years of engineering experience, preferably in medical devices.
  • Demonstrated ability to utilize statistical tools, such as Mini Tab and computer analysis.
Level of Experience

Senior Level

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