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Verification & Validation Test Engineer

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Manchester

On-site

GBP 80,000 - 100,000

25 days ago

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Job summary

Join a forward-thinking company as a Verification and Validation Test Engineer, where your expertise will directly impact the success of innovative medical devices. In this dynamic role, you will develop and write test procedures, assess performance and reliability, and contribute to regulatory submissions. This position offers a unique opportunity to work with a team dedicated to creating life-changing products, ensuring quality and compliance in a fast-paced environment. If you are detail-oriented, self-motivated, and passionate about engineering, this role is perfect for you!

Qualifications

  • BS in relevant fields like Physics or Engineering is essential.
  • Experience in medical devices and FDA regulations is crucial.

Responsibilities

  • Develop and write test procedures for user interfaces and hardware.
  • Contribute to design failure investigations and regulatory submissions.

Skills

Problem Solving

Communication Skills

Data Analysis

Interdisciplinary Teamwork

Self-Motivation

Attention to Detail

Education

Bachelor's in Physics

Bachelor's in Biology

Bachelor's in Engineering (Electrical/Mechanical/Biomedical/Chemical)

Tools

Measurement Instruments

Job description

Job Description

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.


How you will make an impact:

  • 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, you will need the following skills and experience:

  • Must have a BS in Physics, Biology, Electrical, Mechanical, Biomedical Engineering, and/or Chemical 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

About DEKA:

One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern era.

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.

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