Verification & Validation Test Engineer

DEKA Research & Development • Manchester, NH

7h

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. 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 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.

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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 501-1,000 employees