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Junior Verification & Validation Test Engineer

Job in Manchester, Hillsborough County, New Hampshire, 03103, USA
Listing for: DEKA Research & Development
Full Time position
Listed on 2026-07-24
Job specializations:
  • Engineering
    Test Engineer, Quality Engineering, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below

Junior Verification & Validation Test Engineer

DEKA Research and Development, located in Manchester, NH, has an immediate opening for a Junior
Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. Test Engineering is a high‑visibility role with a significant, direct impact on the success of the project.

How you will make an impact as a Junior Verification & Validation Test Engineer:
  • Developing and writing test procedures assessing end‑to‑end performance and reliability of user interfaces and hardware
  • Understanding device design and core technologies in order to inform test method development
  • Determining test coverage for revisions to design
  • Creating and evaluating test fixtures if needed for product design verification
  • Contributing to design failure investigations that may impact Risk Assessments, Hazard Analyses, and FMEAs
  • Contributing toward regulatory and agency submissions
  • Authoring Test Summaries and other documents
Must have the following skills and experience:
  • Must have a BS in Physics, Biology, Electrical, Mechanical, or Biomedical Engineering.
  • Experience with research, development, and product testing
  • Experience writing procedures for others to follow
  • Experience with data and failure analysis
  • Broad measurement instrument knowledge
  • Knowledge and deep understanding of engineering fundamentals
  • Demonstrated problem‑solving ability and techniques
  • Ability to work as part of an interdisciplinary team
  • Self‑motivated and able to self‑prioritize
  • Ability to clearly explain objectives
  • Must be detail oriented and have excellent verbal and written communication skills
  • Experience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO
    13485, and other medical device industry experience preferred
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