Terso Solutions
JOB REQUIREMENTS
Product Design Engineer, IoT - Terso ID 2025-4214 #
Openings: 1
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
Participate in the mechanical and electromechanical design of IoT devices from concept through production, with a focus on performance, reliability, and integration.
Develop detailed engineering documentation, including CAD models, wiring schematics, BOMs, build protocols, and quality control records.
Plan and execute hands‑on hardware prototyping, fabrication, iterative testing, and validation aligned with product and regulatory requirements.
Conduct design iterations, optimization and risk mitigation activities, including Design for Manufacturing, Assembly, Test, etc.
Plan, author, conduct, and document testing and experiments to verify design assumptions, performance, and safety compliance.
Support hardware integration with cloud and connectivity modules through design and physical layout considerations.
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, and QA teams to ensure seamless hardware‑firmware integration.
Work with wider cross‑functional teams to address quality, manufacturability, supportability, and production scaling issues.
Manage project deliverables and milestones, while clearly communicating status, risks, and technical findings to leadership and team stakeholders.
Contribute to risk management and traceability documentation aligned with medical device lifecycle standards where applicable.
Maintain organized records of design revisions, test outcomes, and lessons learned for knowledge sharing and regulatory traceability.
Evaluate and implement new engineering tools and practices, including test and fabrication equipment, design simulation, AI and automation technologies, for future integration.
Demonstrate inclusion through personal actions and accountability for a safe workspace, acting with kindness, curiosity, and respect for others.
Embrace and be open to incorporating Promega’s 6 Emotional & Social competencies to foster a collaborative culture.
APPLICATION INSTRUCTIONS Apply Online:
ipc.us/t/2F71F4D229DD426B
We are proud to be an Equal Opportunity Employer.
Seniority level
Entry level
Employment type
Full‑time
Job function
Engineering and Information Technology
Industries
Hospitals and Health Care
#J-18808-Ljbffr
Openings: 1
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
Participate in the mechanical and electromechanical design of IoT devices from concept through production, with a focus on performance, reliability, and integration.
Develop detailed engineering documentation, including CAD models, wiring schematics, BOMs, build protocols, and quality control records.
Plan and execute hands‑on hardware prototyping, fabrication, iterative testing, and validation aligned with product and regulatory requirements.
Conduct design iterations, optimization and risk mitigation activities, including Design for Manufacturing, Assembly, Test, etc.
Plan, author, conduct, and document testing and experiments to verify design assumptions, performance, and safety compliance.
Support hardware integration with cloud and connectivity modules through design and physical layout considerations.
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, and QA teams to ensure seamless hardware‑firmware integration.
Work with wider cross‑functional teams to address quality, manufacturability, supportability, and production scaling issues.
Manage project deliverables and milestones, while clearly communicating status, risks, and technical findings to leadership and team stakeholders.
Contribute to risk management and traceability documentation aligned with medical device lifecycle standards where applicable.
Maintain organized records of design revisions, test outcomes, and lessons learned for knowledge sharing and regulatory traceability.
Evaluate and implement new engineering tools and practices, including test and fabrication equipment, design simulation, AI and automation technologies, for future integration.
Demonstrate inclusion through personal actions and accountability for a safe workspace, acting with kindness, curiosity, and respect for others.
Embrace and be open to incorporating Promega’s 6 Emotional & Social competencies to foster a collaborative culture.
APPLICATION INSTRUCTIONS Apply Online:
ipc.us/t/2F71F4D229DD426B
We are proud to be an Equal Opportunity Employer.
Seniority level
Entry level
Employment type
Full‑time
Job function
Engineering and Information Technology
Industries
Hospitals and Health Care
#J-18808-Ljbffr