The Senior Systems Verification Engineer will work with the Development team in the system integration and testing of our In Vitro Diagnostic (IVD) products. The Senior Systems Verification Engineer may provide mentorship to other Verification Engineers, and typically works closely with other team members in the system integration and testing of our medical devices. Key Accountabilities Assist with the development of project requirements, support tracing of design inputs to design outputs. Participate in design reviews, develop test automation solutions, and create test plans, test cases, reports, and other deliverables with possible interaction with clinicians, third‑party vendors, manufacturers, and others. Develop verification planning documentation for development projects as needed. Analyze requirements and design specifications from a systems perspective. Develop strategies for system‑level product testing, including software, electrical, analytic, and/or mechanical aspects of the system. Develop system and subsystem test procedures based on product and/or subsystem requirements. Develop test automation and/or test bench component solutions in support of functional and reliability testing with detailed documentation. Participate in hazard and risk analysis. Support design activities and attend design reviews. Create verification reports and overall verification summary reports for systems verification activities. Create work breakdown schedule estimates. Create and execute test plans and procedures. Assist with system integration and debugging as needed. Operate electrical, mechanical, and digital equipment and test fixtures. Work well in a team. May participate in interviews for new department personnel as necessary. May work on process improvement activities. Other duties as assigned with or without accommodation. Networking/Key relationships Research and Development Quality Engineering Minimum Knowledge & Experience required for the position BS/BA degree in CS, EE, ME, Biomedical or related Engineering discipline required. Minimum of seven (7) years of previous experience required; medical device industry experience preferred. Experience in the full development lifecycle for product delivery to market of at least one product required. Skills & Capabilities Testing experience in medical device development or other regulated industry is desired. Experience in elicitation, writing and traceability of system/subsystem requirements for product development is desired. Experience designing and/or creating and utilizing test bench components for system/components testing is desired. Broad technical understanding of multiple disciplines from electrical, mechanical, software is desired. Familiarity with reliability testing is desired. Good communication and presentation skills. Strong planning and organizational skills required. Seniority level Mid‑Senior level Employment type Full‑time Job function Information Technology & Services and Medical Equipment Manufacturing #J-18808-Ljbffr