Senior Systems Engineer – Medical Devices & NPD

Siemens Healthcare; United States; Vor Ort; USD 193.000 - 265.000; Vollzeit

Zusammenfassung

Siemens Healthineers seeks a Senior Systems Engineer for New Product Development to lead system-level engineering across the development lifecycle. You will translate clinical and stakeholder inputs into detailed requirements, architect robust solutions, and guide cross-functional teams through simulations, tests, and design reviews.

The role emphasizes risk management, traceability, and early validation to ensure safe, effective medical devices in a regulated environment.

Qualifikationen

• 10-15+ years of experience in complex electromechanical product development or major redesigns.
• Strong experience in system architecture, requirements engineering, subsystem interfaces, verification, risk management reviews.
• Hands-on experience with multidisciplinary hardware, software and embedded systems.
• Ability to independently lead complex technical investigations and drive cross-functional decisions.

Aufgaben

• Lead systems engineering activities for new product development of Siemens Varian radiation therapy equipment.
• Translate VOC inputs into system and subsystem requirements.
• Develop system architecture, functional decomposition and system specifications; prototype or simulate to de-risk decisions.
• Define and manage interfaces across electrical, electronics, mechanical, software and control subsystems.

Kenntnisse

Systems engineering leadership

Cross-functional collaboration

Requirements engineering

Problem solving

Ausbildung

BS/MS in Electrical Engineering or Systems Engineering

Tools

JAMA

Jobbeschreibung

Siemens Healthineers seeks a Senior Systems Engineer for New Product Development to lead system-level engineering across the development lifecycle. You will translate clinical and stakeholder inputs into detailed requirements, architect robust solutions, and guide cross-functional teams through simulations, tests, and design reviews.

The role emphasizes risk management, traceability, and early validation to ensure safe, effective medical devices in a regulated environment.