What are the responsibilities and job description for the System Engineer position at AVS LLC?
Key Responsibilities • Lead system-level design, development, and integration of medical device products across hardware, software, mechanical, and electrical domains. • Design and review hardware architectures, including sensors, actuators, controllers, and embedded subsystems. • Develop and validate control systems for precise XYZ multi axis mechanical motion, motion profiling, and closed-loop feedback systems. • Collaborate with mechanical engineers to define and validate kinematic designs, tolerances, and movement accuracy for complex electromechanical systems. • Work closely with software teams on embedded and application-level software integration, ensuring seamless interaction with hardware and control systems. • Drive system requirements definition, allocation, traceability, and verification throughout the product lifecycle. • Participate in risk management activities (FMEA, fault analysis) and ensure compliance with medical device standards and regulatory requirements. • Support prototyping, system integration, debugging, verification, and validation testing at component and system levels. • Interface with manufacturing, quality, and regulatory teams to support design transfer and product commercialization. • Provide on-site technical support, issue resolution, and continuous improvement for deployed systems. Requirements and Skills • Bachelor's or master's degree in systems Engineering or Electrical Engineering • Proven experience as a Systems Engineer in medical device development, including full product lifecycle involvement. • Knowledge of Systems design, including analog/digital electronics, sensors, motors, actuators, and embedded platforms. • Hands-on experience with control systems design, modeling, tuning (PID and advanced control), and real-time implementation. • Demonstrated expertise in XYZ mechanical motion systems, precision positioning, robotics, or multi-axis motion control. • Experience integrating software, mechanical, and electrical subsystems into cohesive, reliable products. • Familiarity with medical device regulations and standards (e.g., FDA, IEC 60601, ISO 13485, ISO 14971). • Ability to read and interpret mechanical drawings, electrical schematics, and system block diagrams. • Strong debugging, problem-solving, and root-cause analysis skills in complex electromechanical systems. • Excellent communication and collaboration skills, with the ability to work effectively on cross-functional teams. • Willingness and ability to work onsite in the USA. Good to Have • Experience with MATLAB/Simulink for system modeling, control design, and simulation. • Hands on experience using LabVIEW for test automation, system validation, and data acquisition. • Practical experience with motion controllers (commercial or custom) used in precision positioning systems. Qualification: Bachelor's or master's degree in systems Engineering or Electrical Engineering EXPERTISE AND QUALIFICATIONS Job Description & Skill Requirement: Key Responsibilities • Lead system-level design, development, and integration of medical device products across hardware, software, mechanical, and electrical domains. • Design and review hardware architectures, including sensors, actuators, controllers, and embedded subsystems. • Develop and validate control systems for precise XYZ multi axis mechanical motion, motion profiling, and closed-loop feedback systems. • Collaborate with mechanical engineers to define and validate kinematic designs, tolerances, and movement accuracy for complex electromechanical systems. • Work closely with software teams on embedded and application-level software integration, ensuring seamless interaction with hardware and control systems. • Drive system requirements definition, allocation, traceability, and verification throughout the product lifecycle. • Participate in risk management activities (FMEA, fault analysis) and ensure compliance with medical device standards and regulatory requirements. • Support prototyping, system integration, debugging, verification, and validation testing at component and system levels. • Interface with manufacturing, quality, and regulatory teams to support design transfer and product commercialization. • Provide on-site technical support, issue resolution, and continuous improvement for deployed systems. Requirements and Skills • Bachelor's or master's degree in systems Engineering or Electrical Engineering • Proven experience as a Systems Engineer in medical device development, including full product lifecycle involvement. • Knowledge of Systems design, including analog/digital electronics, sensors, motors, actuators, and embedded platforms. • Hands-on experience with control systems design, modeling, tuning (PID and advanced control), and real-time implementation. • Demonstrated expertise in XYZ mechanical motion systems, precision positioning, robotics, or multi-axis motion control. • Experience integrating software, mechanical, and electrical subsystems into cohesive, reliable products. • Familiarity with medical device regulations and standards (e.g., FDA, IEC 60601, ISO 13485, ISO 14971). • Ability to read and interpret mechanical drawings, electrical schematics, and system block diagrams. • Strong debugging, problem-solving, and root-cause analysis skills in complex electromechanical systems. • Excellent communication and collaboration skills, with the ability to work effectively on cross-functional teams. • Willingness and ability to work onsite in the USA. Good to Have • Experience with MATLAB/Simulink for system modeling, control design, and simulation. • Hands on experience using LabVIEW for test automation, system validation, and data acquisition. • Practical experience with motion controllers (commercial or custom) used in precision positioning systems. Qualification: Bachelor's or master's degree in systems Engineering or Electrical Engineering
Salary.com Estimation for System Engineer in Dublin, CA
$130,423 to $159,933
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