Product Design Engineer IoT Terso

JOB REQUIREMENTS: Job Description JOB OBJECTIVE: Design and develop thephysical hardware for connected IoT devices that enable intelligent,real-time solutions in healthcare and other markets as needed. Focus ondelivering robust, manufacturable, and regulatory-compliant hardwareproducts while partnering across disciplines to ensure seamless systemintegration within IoT environments. As market demands evolve, this rolemay contribute to the development of medical devices, requiringalignment with FDA and international regulatory standards. Implementemerging tools and practices, including AI and automation. COREDUTIES: 1. Participate in the mechanical and electromechanical design ofIoT devices from concept through production, with a focus onperformance, reliability, and integration. 2. Develop detailedengineering documentation, including CAD models, wiring schematics,BOMs, build protocols, and quality control records. 3. Plan and executehands-on hardware prototyping, fabrication, iterative testing, andvalidation aligned with product and regulatory requirements to meetproduct development timelines. 4. Conduct design iterations,optimization and risk mitigation activities, including Design forManufacturing, Assembly, Test, etc. 5. Plan, author, conduct, anddocument testing and experiments to verify design assumptions,performance, and safety compliance. 6. Support hardware integration withcloud and connectivity modules through design and physical layoutconsiderations. 7. Assist with hardware certification and complianceprocesses for global standards such as FCC, CE, ISO, and potentially FDA21 CFR Part 820 or ISO 13485 for future medical devices. 8. Collaboratewith other colleagues, firmware, QA teams to ensure seamlesshardware-firmware integration. 9. Work with wider cross-functional teamsto address quality, manufacturability, supportability, and productionscaling issues. 10. Manage project deliverables and milestones, whileclearly communicating status, risks, and technical findings toleadership and team stakeholders. 11. Contribute to risk management andtraceability documentation aligned with medical device lifecyclestandards where applicable. 12. Maintain organized records of designrevisions, test outcomes, and lessons learned for knowledge sharing andregulatory traceability. 13. Evaluate and implement new engineeringtools and practices, including test and fabrication equipment, designsimulation, AI and automation technologies, for future integration. 14.Demonstrates inclusion through their own words and actions and isaccountable for a safe workspace. Acts with kindness,... For full infofollow application link. Diversity is important at Promega. We are proudto be an Equal Opportunity Employer, and make employment decisionswithout regard to race, color, religion, sex, sexual orientation, genderidentity, national origin, veteran status, disability, or any otherprotected class. APPLICATION INSTRUCTIONS: Apply Online:ipc.us/t/1A7B5889CE1F4726 Qualified females, minorities, and specialdisabled veterans and other veterans are encouraged to apply.

Created: 2025-12-18