Product Design Engineer IoT Terso

JOB REQUIREMENTS: Product Design Engineer, IoT - Terso ID 2025-4214 #of Openings 1 Category Engineering Job Description JOB OBJECTIVE: Designand develop the physical hardware for connected IoT devices that enableintelligent, real-time solutions in healthcare and other markets asneeded. Focus on delivering robust, manufacturable, andregulatory-compliant hardware products while partnering acrossdisciplines to ensure seamless system integration within IoTenvironments. As market demands evolve, this role may contribute to thedevelopment of medical devices, requiring alignment with FDA andinternational regulatory standards. Implement emerging tools andpractices, including AI and automation. CORE DUTIES: 1. Participate inthe mechanical and electromechanical design of IoT devices from conceptthrough production, with a focus on performance, reliability, andintegration. 2. Develop detailed engineering documentation, includingCAD models, wiring schematics, BOMs, build protocols, and qualitycontrol records. 3. Plan and execute hands-on hardware prototyping,fabrication, iterative testing, and validation aligned with product andregulatory requirements to meet product development timelines. 4.Conduct design iterations, optimization and risk mitigation activities,including Design for Manufacturing, Assembly, Test, etc. 5. Plan,author, conduct, and document testing and experiments to verify designassumptions, performance, and safety compliance. 6. Support hardwareintegration with cloud and connectivity modules through design andphysical layout considerations. 7. Assist with hardware certificationand compliance processes for global standards such as FCC, CE, ISO, andpotentially FDA 21 CFR Part 820 or ISO 13485 for future medical devices.8. Collaborate with other colleagues, firmware, QA teams to ensureseamless hardware-firmware integration. 9. Work with widercross-functional teams to address quality, manufacturability,supportability, and production scaling issues. 10. Manage projectdeliverables and milestones, while clearly communicating status, risks,and technical findings to leadership and team stakeholders. 11.Contribute to risk management and traceability documentation alignedwith medical device lifecycle standards where applicable. 12. Maintainorganized records of design revisions, test outcomes, and lessonslearned for knowledge sharing and regulatory traceability. 13. Evaluateand implement new engineering tools and practices, including test andfabrication equipment, design simulation, AI and automationtechnologies, for future integration. 14. Demonstrates inclusion throughtheir own words and actions and is accountable for a safe workspace.Acts with kindness, curiosity, and respect for others. 15. Embracing andbeing open to incorporating Promega's 6 Emotional & Social... For fullinfo follow application link. We are proud to be an Equal OpportunityEmployer. APPLICATION INSTRUCTIONS: Apply Online:ipc.us/t/2F71F4D229DD426B

Created: 2025-12-26