What are the responsibilities and job description for the Product Design Engineer IoT Terso position at Terso Solutions?
JOB REQUIREMENTS: Product Design Engineer, IoT - Terso ID 2025-4214 \#
of Openings 1 Category Engineering Job Description JOB OBJECTIVE: Design
and develop the physical hardware for connected IoT devices that enable
intelligent, real-time solutions in healthcare and other markets as
needed. Focus on delivering robust, manufacturable, and
regulatory-compliant hardware products while partnering across
disciplines to ensure seamless system integration within IoT
environments. As market demands evolve, this role may contribute to the
development of medical devices, requiring alignment with FDA and
international regulatory standards. Implement emerging tools and
practices, including AI and automation. CORE DUTIES: 1. Participate in
the mechanical and electromechanical design of IoT devices from concept
through production, with a focus on performance, reliability, and
integration. 2. Develop detailed engineering documentation, including
CAD models, wiring schematics, BOMs, build protocols, and quality
control records. 3. Plan and execute hands-on hardware prototyping,
fabrication, iterative testing, and validation aligned with product and
regulatory 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 design
assumptions, performance, and safety compliance. 6. Support hardware
integration with cloud and connectivity modules through design and
physical layout considerations. 7. Assist with hardware certification
and compliance processes for global standards such as FCC, CE, ISO, and
potentially FDA 21 CFR Part 820 or ISO 13485 for future medical devices.
cross-functional teams to address quality, manufacturability,
supportability, and production scaling issues. 10. Manage project
deliverables and milestones, while clearly communicating status, risks,
and technical findings to leadership and team stakeholders. 11.
Contribute to risk management and traceability documentation aligned
with medical device lifecycle standards where applicable. 12. Maintain
organized records of design revisions, test outcomes, and lessons
learned for knowledge sharing and regulatory traceability. 13. Evaluate
and implement new engineering tools and practices, including test and
fabrication equipment, design simulation, AI and automation
technologies, for future integration. 14. Demonstrates inclusion through
their own words and actions and is accountable for a safe workspace.
Acts with kindness, curiosity, and respect for others. 15. Embracing and
being open to incorporating Promega\'s 6 Emotional & Social\... For full
info follow application link. We are proud to be an Equal Opportunity
Employer. \*\*\*\*\* APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/2F71F4D229DD426B
of Openings 1 Category Engineering Job Description JOB OBJECTIVE: Design
and develop the physical hardware for connected IoT devices that enable
intelligent, real-time solutions in healthcare and other markets as
needed. Focus on delivering robust, manufacturable, and
regulatory-compliant hardware products while partnering across
disciplines to ensure seamless system integration within IoT
environments. As market demands evolve, this role may contribute to the
development of medical devices, requiring alignment with FDA and
international regulatory standards. Implement emerging tools and
practices, including AI and automation. CORE DUTIES: 1. Participate in
the mechanical and electromechanical design of IoT devices from concept
through production, with a focus on performance, reliability, and
integration. 2. Develop detailed engineering documentation, including
CAD models, wiring schematics, BOMs, build protocols, and quality
control records. 3. Plan and execute hands-on hardware prototyping,
fabrication, iterative testing, and validation aligned with product and
regulatory 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 design
assumptions, performance, and safety compliance. 6. Support hardware
integration with cloud and connectivity modules through design and
physical layout considerations. 7. Assist with hardware certification
and compliance processes for global standards such as FCC, CE, ISO, and
potentially FDA 21 CFR Part 820 or ISO 13485 for future medical devices.
- Collaborate with other colleagues, firmware, QA teams to ensure
cross-functional teams to address quality, manufacturability,
supportability, and production scaling issues. 10. Manage project
deliverables and milestones, while clearly communicating status, risks,
and technical findings to leadership and team stakeholders. 11.
Contribute to risk management and traceability documentation aligned
with medical device lifecycle standards where applicable. 12. Maintain
organized records of design revisions, test outcomes, and lessons
learned for knowledge sharing and regulatory traceability. 13. Evaluate
and implement new engineering tools and practices, including test and
fabrication equipment, design simulation, AI and automation
technologies, for future integration. 14. Demonstrates inclusion through
their own words and actions and is accountable for a safe workspace.
Acts with kindness, curiosity, and respect for others. 15. Embracing and
being open to incorporating Promega\'s 6 Emotional & Social\... For full
info follow application link. We are proud to be an Equal Opportunity
Employer. \*\*\*\*\* APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/2F71F4D229DD426B