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Staff Systems Verification Engineer (Smith & Nephew, Inc., Andover, MA): Drive and lead system verification efforts in partnership with the Systems Engineering and R&D New Product Development teams. Autonomously lead large scale projects’ test activities, allocate test equipment and materials, and align with Program Management and multi-functional teamwork and timeline. Act as a Subject Matter Expert (SME) in leading and supporting test stands software automation and scripting. Support the systems engineers with definition of new products by implementing operational profiles, preparing for test, dry-run, executing test, tracing requirements to test cases and guiding the test strategy. Support troubleshooting and root causing of Systems defects and enable R&D team to identify fixes. Plan, develop and execute software testing (both manual and automated) for medical devices, based on context and risks associated with the project.
Monday – Friday, 40 hours per week.
MINIMUM REQUIREMENTS:
Must have a Bachelor’s degree in Electrical Engineering, Biomedical Engineering, Computer Engineering, Computer Science or related field plus 6 years of post-baccalaureate experience in the job offered or related role in the Medical Device industry. Alternatively, will accept a Master’s degree in Electrical Engineering, Biomedical Engineering, Computer Engineering, Computer Science or related field plus 3 years of experience in the job offered or related role in the Medical Device industry.
Of the required experience, must have 3 years of experience in each of the following:
· Test Development involving test planning, authoring, executing, and reporting.
· Tests revision control management solution experience such as: JAMA, Cockpit, Azure DevOps or Helix/TestTrack.
· Industry experience in test scripting using Python.
· Embedded systems (combining microprocessors or microcontroller) design or test experience.
· Test experience with one or more of the interface communications buses: CAN, RS232, USB, I2C, SPI, or PCIexpress.
· Medical device industry, where one of the following is applied: FDA Good Manufacturing Practice, FDA 21 CFR Part 820 or ISO 13485:2016.
· Full lifecycle of product test including evaluation of requirement for testability, test protocol drafting, protocol dry run, formal protocol execution, test report generation and release into document control.
· Using defects management systems such as: JIRA, Bugzilla, Azure, or ClearCase.
· Identifying, troubleshooting, and validating fixes for failures.
· Driving or supporting requirements creation and reviews for systems design inputs and sub-system requirements.
Of the required experience, must have 2 years of experience in each of the following:
· Analog and digital circuits, microprocessor hardware, and software (industry experience or graduate-level educational course work acceptable).
· Failure Mode & Effects Analysis for medical device systems and sub-components.
Of the required experience, must have 1 year of industry experience or graduate-level educational course work in MATLAB or Simulink and LabVIEW.
Must be willing and able to travel up to 10% domestically to visit other Smith & Nephew offices, as needed.
How to apply: Apply online at https://www.smith-nephew.com/careers/ click on vacancies and search Staff Systems Verification Engineer (REQ: R72595).
