Verification & Validation Test Engineer at DEKA Research & Development

Manchester, New Hampshire, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Sep, 26

Salary

0.0

Posted On

14 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Verification and Validation, Test Procedure Development, Data Analysis, Failure Analysis, Measurement Instruments, Problem Solving, Interdisciplinary Collaboration, Technical Communication, Medical Device Testing, FDA QSR Knowledge, ISO 13485, Risk Assessment, Hazard Analysis, FMEA, Test Fixture Creation, Regulatory Submissions

Industry

Biotechnology Research

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 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 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 age. 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.

Responsibilities

Develop and execute test procedures to assess the performance and reliability of medical device hardware and user interfaces. Contribute to design failure investigations, risk assessments, and regulatory submissions through detailed test summaries.