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HCLTech
Test Lead
Career Insights for Ergonomist
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Based on Mississippi data
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What they do
An Ergonomist designs workplace furniture and equipment or tools to make them safe, efficient and comfortable to use, and to minimize strain for workers. Incorporates occupational health criteria in design. Advises on design for products, such as computers, as they are being developed, or advises on the re-design of an office space or factory process to improve productivity and safety.
$91,270 / year median in Mississippi
+13% projected growth
Job Description
Lake, Illinois Job Summary As a part of the Design Validation Team, the Registered Nurse (RN) is a key stakeholder of device design and development team. In this role The RN is responsible for providing clinical expertise to support the design validation of infusion pump systems. This role ensures that products are safe, effective, and meet user needs by participating in human factors evaluations, simulated-use testing, and clinical workflow validation activities. The RN collaborates cross-functionally with engineering, human factors, quality, regulatory, and clinical teams to represent the voice of the end user throughout product development. Key Responsibilities Clinical Expertise & User Representation Serve as a clinical subject matter expert (SME) for infusion therapy practices, workflows, and patient safety considerations Translate real-world clinical use into design input and validation requirements Ensure device usability aligns with nursing workflows and standards of care Design Validation Activities Plan, develop, and execute design validation studies, including simulated-use and usability testing Participate in formative and summative human factors evaluations Support protocol development, test execution, and data collection Evaluate whether product design meets intended use and user needs Testing & Simulation Conduct hands-on testing of infusion pump systems in simulated and controlled environments Identify use-related risks, potential errors, and opportunities for design improvement Provide detailed observations and documentation of user interactions with devices Documentation & Compliance Author and review validation protocols, reports, and test documentation in accordance with regulatory standards (FDA, ISO 13485, IEC 62366, etc.) Ensure compliance with design control requirements and quality system procedures Support audit readiness and regulatory submissions as needed Cross-Functional Collaboration Partner with engineering, quality, risk management, and human factors teams Contribute to risk analyses (e.g., use-related risk assessments, FMEA) Provide input to design reviews and development milestones Training & Support Assist in development of training materials, instructions for use (IFU), and labeling Support internal teams by educating on clinical workflows and infusion therapy practices Maximum Salary (US): 128000 Minimum Salary (US): 69000 #body.unify div.unify-button-container .