Senior Test Engineer - medical devices

  • InnoTech Staffing
  • Manchester, New Hampshire
  • 04/24/2026
Full time Information Technology Telecommunications Testing

Job Description

Job DescriptionJob Description

InnoTECH Staffing is looking to hire a Senior Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct impact on the success of our projects. It will be a great opportunity to work on some amazing projects that make a positive impact on the world.

This requires being onsite 5 days a week in Manchester, NH.

There is no sponsorship.

How you will make an impact as a Senior Test Engineer:

  • Writing test plans, test procedures and other activities involving performance, durability, and reliability assessments

  • Understand device design and core technologies in order to inform test method development

  • Determining test coverage for revisions to design

  • Creating and evaluating test fixtures needed for product design verification

  • Contributing to design failure investigations that may impact Risk Assessment, Hazard Analysis, and FTAs

  • Participating and contributing toward regulatory and agency submissions

  • Authoring Quality Plans, Test Summaries, and other documents

What you need to be successful Senior Test Engineer:

  • BS in Biomedical, Mechanical and/or Robotics/ Automation Engineering

  • 3+ years' experience testing electro-mechanical devices (medical devices preferred)

  • Must have laboratory/ wet lab skills and experience

  • Must have fluid system handling experience

  • Leadership and/or mentoring experience

  • Knowledge and deep understanding of engineering fundamentals

  • Capability to create and clearly explain team objectives and write procedures for others to follow

  • Demonstrated problem solving ability and techniques

  • Ability to work as part of an interdisciplinary team

  • Self-motivated and able to self-prioritize

  • Must have excellent verbal and written communication skills

Preferred skills and experience:

  • Knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience

  • Experience with research, development, and product testing

  • Experience writing procedures for others to follow

  • Experience with data and failure analysis

  • Broad measurement instrument knowledge