Verification & Validation Test Engineer

DEKA Research & DevelopmentManchester, NH
1dOnsite

About The Position

DEKA Research and Development, located in Manchester, NH, has an immediate opening for a Verification and 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. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

Requirements

  • 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

Nice To Haves

  • Experience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred

Responsibilities

  • 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
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