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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Systems Test Engineer - **Company:** Elucent Medical, Inc. - **Location:** Eden Prairie, MN, United States - **Experience:** Starter - **Salary:** $65,000.0 - $75,000.0 - **Contract:** Permanent contract - **Skills:** Data Analysis, Application Lifecycle Management, Systems Engineering, Microsoft Azure, Code Coverage, Desktop Computing, Document Management Systems, Formal Verification, Human-Computer Interaction, Python (Programming Language), Software Tools, Requirements Traceability, Software Requirements Analysis, Verification and Validation (Software), Test Data, Scripting, Information Technology - **Published:** June 29, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=32cc5c56796fdce8 ## About the Role Do you have experience in UI?, * Required: Bachelor's degree in Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Systems Engineering, Computer Science, Physics, Mathematics, or a related technical field. * Required: 0-2 years of relevant engineering, test, verification/validation, quality, software, hardware experience. * Required: Ability to follow approved procedures, document objective evidence, apply good documentation practices, and escalate quality, safety, regulatory or technical concerns. * Preferred: Experience working with complex systems involving software, hardware, electrical, mechanical, user interface, and human factors. * Preferred: Experience developing and executing test protocols, engineering studies, and verification activities. * Preferred: Experience verifying software changes and documenting defects using Azure DevOps or a similar lifecycle management tool. * Preferred: Experience with data collection, analysis, scripting, automation, laboratory instrumentation, test fixtures, or data acquisition systems. * Preferred: navigation, imaging, or other medical device experience with exposure to design verification and validation, risk management, or requirements traceability. * Preferred: Exposure to medical device design controls, verification and validation, ISO 13485, ISO 14971, IEC 62304, IEC 62366-1, requirements traceability, risk management or regulated product development., * Ability to perform assigned testing in accordance with FDA QMSR / 21 CFR Part 820, ISO 13485, ISO 14971, company SOPs, good documentation practices, and approved test procedures. * Strong analytical, systems-thinking, and problem-solving skills. * Ability to understand interactions between software, hardware, electrical, mechanical, user interface, and clinical use elements. * Ability to design, execute, troubleshoot, and document system-level engineering tests. * Strong documentation skills, including protocols, reports, engineering summaries, defect documentation, and verification evidence, and traceability records. * Ability to interpret requirements, user needs, risk controls, intended-use scenarios, and design inputs. * Ability to verify software changes, document findings, analyze test data, identify trends, and communicate technical conclusions. * Ability to use or develop scripts, automation tools, data-analysis utilities, or engineering tools; Python experience preferred. * Ability to support prototype evaluation, test-method development, technical exploration, and innovation activities in addition to formal verification and validation work. * Ability to work independently with general direction, collaborate cross-functionally, prioritize assigned work, follow quality-system procedures, and escalate risks appropriately. Physical Requirements / Work Conditions: * Ability to work in office and laboratory environments. * Frequent use of computers, software tools, laboratory instrumentation, test equipment, fixtures, data-acquisition systems, and standard office equipment. * Ability to perform hands-on testing, including setup, operation, and troubleshooting. * Ability to sit, stand, walk, bend, reach, and perform bench-level engineering work for extended periods as needed. * May require occasional lifting, carrying, pushing, or pulling of equipment, fixtures, materials, or test components up to 25 pounds. ## Description * Develop, maintain, and execute system-level verification and validation test protocols for medical device systems in accordance with approved protocols, acceptance criteria, company SOPs, good documentation practices, and applicable FDA/ISO quality-system requirements. * Design and perform challenge testing for complex clinical workflows, edge cases, realistic use conditions, and risk scenarios. * Review requirements, user needs, risk controls, and intended-use scenarios to support test coverage, acceptance criteria, and traceability. * Verify software changes, defects, and work items using Azure DevOps or similar lifecycle management tools; document findings, verification evidence, unresolved anomalies and investigation results in appropriate records. * Identify, document, investigate, and escalate anomalies, test deviations, nonconforming results, usability issues, workflow gaps, performance concerns, and unexpected system behavior. * Troubleshoot and resolve system interactions involving software, hardware, RF environments, and instrumentation. * Use scripts, Python-based tools, automation, and data-analysis workflows to support testing, investigations, and engineering decisions. * Execute testing in accordance with approved procedures, quality-system requirements, applicable standards, and good documentation practices. * Collaborate with systems, software, electrical, mechanical, quality, regulatory, clinical, manufacturing, and leadership personnel through design reviews, risk reviews, requirements reviews, defect reviews, and software change reviews. * Support innovation efforts through prototype evaluation, data analysis, exploratory testing, and technical feedback sessions to improve and expand the product portfolio. * Support manufacturing, field service, and post-market investigations as assigned. ## Related Videos - [JavaScript? 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