Verification & Validation Test Engineer - medical device

InnoTech Staffing • Manchester, NH

22h • Onsite

About The Position

InnoTECH Staffing is seeking a Verification & Validation Test Engineer for a dynamic medical device research and development environment in Manchester, New Hampshire. This high-visibility role will contribute directly to project success and involve work on projects intended to make a positive impact. The position is full-time and permanent, with five days per week onsite. Applicants must be U.S. citizens or permanent residents.

Requirements

• Bachelor of Science in Biomedical, Mechanical, Electrical, Robotics, and/or Automation Engineering.
• At least 3 years of experience testing electromechanical devices; medical device experience is preferred.
• Fluid system handling experience.
• Leadership and/or mentoring experience.
• Knowledge and deep understanding of engineering fundamentals.
• Ability 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 prioritize work independently.
• Excellent verbal and written communication skills.
• Must be a U.S. citizen or permanent resident.

Nice To Haves

• Knowledge of FDA Quality System Regulations (QSRs), ISO 13485, and/or 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 knowledge of measurement instruments.

Responsibilities

• Write test plans, test procedures, and other materials for performance, durability, and reliability assessments.
• Understand device design and core technologies to inform test method development.
• Determine test coverage for design revisions.
• Create and evaluate test fixtures for product design verification.
• Contribute to design failure investigations that may affect risk assessments, hazard analyses, and fault tree analyses (FTAs).
• Participate in and contribute to regulatory and agency submissions.
• Author quality plans, test summaries, and other documents.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level