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R&D Test Engineer Entry Level

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
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: R&D Test Engineer [Entry Level]

Position

R&D Test Engineer [Entry Level]

Location

Franklin Lakes, NJ

Duration

12+ Months Contract

Total Hours/week

40.00

Shift

1st Shift

Client

Medical Device Company

Employment Type

Contract on W2 (Need US Citizens Or GC Holders Only)

Visa

No H1B’s

Description

For the hardware tester position, it has to be local FLKS site. For testing, needs to be in lab every week day.

The R&D test engineer position is an entry level position, responsible for hardware testing activities to develop and commercialize complex instrumentation in the medication safety space.

The R&D test engineer will support engineering studies and Design Verification activities for the Intelliport products including disposable sensors and several reusable electro‑mechanical devices. In addition to testing, this associate may also contribute to the improvement of testing methods, measurement system development & analysis of test methods, the improvement of fixtures, data processing and analysis. The testing performed in this role will help ensure that our products meet our customer’s expectations and regulatory requirements.

Knowledge of disciplined product development processes, regulatory, quality requirements and design controls, such as 21 CFR 820.30 is a plus.

Minimum Qualifications
  • Bachelor’s degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering, Applied Physics or similar
  • Proficient in reading and understanding assembly drawings, manufacturing and test instructions, and service manuals.
Desired Qualifications
  • Experience testing medical device product for Design Verification
  • Knowledge on testing software, firmware and hardware by following test protocols
  • Working knowledge of regulatory standards applicable to design of medical devices, including FDA QSR, ISO 13845, ISO 14971 and IEC 60601 and collateral standards
  • Post-educational experience in Medical Device Design
  • Design for Six Sigma, Design for Manufacturability and Reliability training / experience
  • Graduate degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering or Applied Physics
  • Fluent in CAD modeling such as Solidworks or ProE
Competencies
  • Excellent written & verbal communication skills
  • Self-directed with the ability to learn and adapt quickly to new technologies and trends
  • Strong organization and coordination skills

    Ability to work independently after appropriate direction
  • Careful, deliberate, disciplined, meticulous, and well organized in performing laboratory tests and recording results
  • Ability to read and follow Standard Operation Procedures, Good laboratories Practices, Good Documentation Practices knowledge
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Position Requirements
Less than 1 Year work experience
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