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Verification and Validation Test Engineer - V&V, medical device

InnoTech Staffing
locationManchester, NH, USA
PublishedPublished: 6/14/2022
Manufacturing
Full Time

Job Description

Job Description

InnoTECH Staffing has an immediate opening for a Verification and Validation Test Engineer to work in a dynamic medical device R&D environment located onsite 5 days a week in Manchester, NH.

*** Candidate must be a US Citizen or Greencard holder.

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 Verification and 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

To be successful in this role as a Verification and Validation Test Engineer, you will need 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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