Design Verification Engineer

Company:  Ventura Solutions Inc.
Location: Portsmouth
Closing Date: 18/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description

Are you a Design Verification Automation Engineer looking for a new opportunity? In this position, you will have the opportunity to work with an innovative firm.

Ventura Solutions is a trusted medical device and pharmaceutical staffing, consulting, and training firm. We believe that the best way to advance healthcare is through innovation and continuous improvement. We value our commitment to solving healthcare's toughest problems and delivering world-class products, services, and human resource solutions. We are a company of problem solvers, inventors, teachers, and friends.

The Design Verification Automation Engineer is responsible for planning, executing and documentation of verification efforts for our client's proprietary software, firmware and connected, proprietary Medical Devices. S/he will work amongst a cross-functional team with the goal of understanding the assigned work and improving products. As a solution-oriented individual, they will help drive effectiveness, efficiency, and compliance within the team. Ability to establish time estimates and schedules and provide clear and concise status updates to leadership teams as required, as well as to be able to show progress vs. overall project goals

Responsibilities

  • Review, assess and provide recommendations on current test verification activities against compliance to FDA/ISO guidelines.
  • Works with leadership and development teams to establish best practices.
  • Establish and update process and procedures for Design Verification including identifying any new or necessary tools
  • Assist in the refinement of requirements and user stories to ensure verification perspectives are incorporated.
  • Demonstrate high proficiency in test case development for system testing.
  • Deliver high quality, compliant test plans and test cases utilizing Microsoft TFS/Azure DevOps, Microsoft Test Manager and supporting tools.
  • Design, implement and execute both manual and automated test cases.
  • Assist in the definition of system level test strategies.
  • Assist in the design and development of test systems required for verification.
  • Participates in requirements development, systems level document reviews.
  • Defect logging, tracking and reproduction (bugs).
  • Provide feedback to improve various Verification-involved process.
  • Bug reproduction, logging, and triage.
  • Occasional project management of development projects.
  • Identify obstacles, meet deadlines.
  • Additional work as assigned.

Qualifications

  • Bachelor’s degree in Engineering (Systems, Electrical/Electronic, Mechanical, Biomedical, or equivalent).
  • Medical device or device design, development and testing experience is preferred.
  • 3+ years relevant work experience in related field
  • Excellent cross-functional skills.
  • Experience with Agile testing methodology.
  • Experience with Microsoft TFS/Azure DevOps, Microsoft Test Manager (MTM) is an asset.
  • Experience in an automated test environment is an asset.
  • Experience automating tests with C#, .NET and Azure DevOps. is an asset.
  • Excellent verbal and written communication skills (English).
  • Experience testing and troubleshooting peripheral device communication and connectivity (Bluetooth/USB).
  • Experience testing systems in a regulated industry user/patient safety is preferred (e.g., medical device, automotive, aerospace).
  • Experience with FDA’s Quality System Regulation (CFR 820) and/or ISO 13485 is preferred.

Location

  • Portsmouth, NH

Employment Type

  • W2 employee, contract and/or contract to hire

Benefits for W2 Employees

  • Choice of medical, dental, and vision plans.
  • Paid vacation time.
  • Competitive hourly rate.
  • 401(k)

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

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