Test Engineer - Verification & Validation - medical device

InnoTech Staffing • Manchester, NH

1d • Onsite

About The Position

InnoTECH Staffing has an immediate opening for a Test Engineer to work in a dynamic medical device R&D environment at our client who is located in Manchester, NH. This requires being onsite 5 days a week and 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

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
• Must be a US Citizen or Greencard holder

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