Systems Engineer

Role: Systems Engineer
Location: Dublin California (Onsite)
Duration: Permanent (Full Time)

Job Description:

Simple Summary: A Systems Engineer acts as the master coordinator of a complex product. Imagine building a modern medical device is like building a car-there are mechanical parts electronics motors software sensors and quality requirements. The Systems Engineer ensures all these parts work together correctly. Daily responsibilities include translating customer needs into technical requirements coordinating engineering teams managing product risks validating system performance supporting testing and ensuring regulatory compliance. The company hires this role to make sure products are reliable safe compliant and function exactly as intended before reaching customers. Example: If a medical imaging device needs motors sensors software and precision movement the Systems Engineer ensures every subsystem communicates properly and meets performance targets. Technologies include System Engineering Requirements Management Risk Management Motion Control Systems Electromechanical Design Embedded Systems FPGA Microcontrollers MATLAB/Simulink and Medical Device Standards.

Responsibilities:

• Systems Engineering & Product Development
• Lead system architecture design integration and validation activities.
• Translate customer and business needs into system requirements.
• Manage requirements allocation traceability verification and validation.
• Drive product development throughout the complete lifecycle from concept through commercialization.
• Coordinate onsite and offshore engineering teams.
• Electromechanical Systems
• Design and review systems involving sensors actuators controllers motors and embedded platforms.
• Develop and validate motion control systems including multi-axis XYZ positioning systems.
• Support control system tuning feedback loops and performance optimization.
• Collaborate with mechanical teams on tolerances kinematics and movement accuracy.
• Software & Hardware Integration
• Work with embedded and application software teams.
• Integrate software electrical and mechanical subsystems.
• Support system debugging troubleshooting and root cause analysis.
• Ensure reliable interaction between hardware and software components.
• Quality & Risk Management
• Lead risk management activities including FMEA and fault analysis.
• Support compliance with FDA IEC 60601 ISO 13485 and ISO 14971 standards.
• Participate in verification and validation testing.
• Support design transfer manufacturing readiness and commercialization activities.
• Cross-Functional Collaboration
• Partner with Manufacturing Quality Regulatory R&D and Operations teams.
• Provide technical support for deployed systems.
• Drive continuous improvement initiatives.
• Required Qualifications
• Bachelors or Masters Degree in Systems Engineering or Electrical Engineering.
• 10-15 years of Systems Engineering experience.
• Experience in complete product development lifecycle.
• Strong requirements management and traceability experience.
• Risk Management and FMEA expertise.
• Medical Device development experience.
• Experience with electromechanical systems and system integration.
• Knowledge of sensors motors actuators embedded platforms and control systems.
• Strong communication and stakeholder management skills.
• Experience working with global teams and onsite-offshore coordination.

Nice to Have:

• MATLAB
• Simulink
• LabVIEW
• FPGA
• Microcontrollers
• Model-Based Systems Engineering (MBSE)
• Advanced Motion Control Systems