Electrical Engineer

Key Responsibilities

• Lead electrical system and subsystem design for medical devices.
• Translate user, clinical and business requirements into system specifications.
• Design electrical schematics, PCB layouts and supporting documentation using ECAD tools.
• Develop analog, digital, power supply, isolation and signal conditioning circuitry.
• Design and validate embedded control systems, motor controls and power delivery systems.
• Collaborate with firmware and software engineers.
• Support sensor integration and communication interfaces (USB, HDMI, Ethernet, wireless/RF).
• Lead verification, validation and testing activities.
• Conduct electrical and functional testing using laboratory instruments.
• Ensure compliance with IEC 60601, EMC/EMI and other applicable standards.
• Lead design FMEAs, risk assessments and hazard analyses.
• Maintain Design History Files (DHF) and technical documentation.
• Support regulatory submissions including 510(k) and CE Mark documentation.
• Work with third-party testing laboratories.
• Mentor junior engineers and technicians.
• Lead root cause analysis and corrective actions.
• Ensure compliance with ISO 13485 and company quality systems. [Manpower R...ctrical_V1 | PDF]

Requirements

Education

• Bachelor's degree in Electrical Engineering, Electronics Engineering, Computer Engineering or related field. [Manpower R...ctrical_V1 | PDF]

Experience

• 6 to 9 years of experience in electrical design, embedded systems or R&D engineering.
• Medical device industry experience is highly desirable, particularly surgical, endoscopic, imaging or electromechanical products. [Manpower R...ctrical_V1 | PDF]

Skills

• Schematic capture, PCB layout and ECAD tools.
• Analog, digital, mixed-signal and embedded systems design.
• Use of oscilloscopes, logic analysers, spectrum analysers and multimeters.
• Motor control, power delivery and sensor integration.
• Communication protocols such as USB, HDMI, Ethernet, CAN, SPI and I2C.
• Knowledge of IEC 60601-1, IEC 60601-1-2, ISO 14971 and FDA 21 CFR 820.
• Knowledge of 510(k), CE Mark and global medical device regulations.
• Strong written and verbal communication skills.
• Root cause investigation and problem-solving capabilities.