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Senior Design Verification Engineer

Job in Manchester, Hillsborough County, New Hampshire, 03103, USA
Listing for: DEKA Research & Development
Full Time position
Listed on 2026-06-02
Job specializations:
  • Engineering
    Biomedical Engineer, Electronics Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 110000 USD Yearly USD 80000.00 110000.00 YEAR
Job Description & How to Apply Below

DEKA Research & Development, located in Manchester, NH, is seeking a Senior Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with adirect impact on the success of our projects. It will be a great opportunity to work on some amazing projects that make a positive impact on the world. Do you want to make a difference with your work?

At DEKA you can!

How you will make an impact as a Senior Design Verification Engineer
  • Writing test plans, test procedure sand other activities involving performance, durability, and reliability assessments
  • Understand device design and core technologies in order to inform test method development
  • Determining test coverage for revisions to design
  • Creating and evaluating test fixtures needed for product design verification
  • Contributing to design failure investigations that may impact Risk Assessment, Hazard Analysis, and FTAs
  • Participating and contributing toward regulatory and agency submissions
  • Authoring Quality Plans, Test Summaries, and other documents
What you need to be successful Senior Design Verification Engineer
  • BS in Biomedical, Mechanical and/or Robotics/ Automation Engineering
  • 3+ years' experience testingelectro-mechanical devices (medical devices preferred)
  • Must have laboratory/ wet lab skills and experience
  • Must have fluid system handling experience
  • Leadership and/or mentoring experience
  • Knowledge and deep understanding of engineering fundamentals
  • Capability to create and clearly explain team objectives and write procedures for others to follow
  • Demonstrated problem solving ability and techniques
  • Ability to work as part of an interdisciplinary team
  • Self-motivated and able to self-prioritize
  • Must have excellent verbal and written communication skills
Preferred skills and experience
  • Knowledge of FDAQuality System Regulations (QSRs) and/or ISO
    13485, and other medical device industry experience
  • Experience with research, development, and product testing
  • Experience writing procedures for others to follow
  • Experience with data and failure analysis
  • Broad measurement instrument knowledge
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Position Requirements
10+ Years work experience
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