Senior Electronic Engineer

- Work Experience Requirement: 5-10 years

- Job Objective: Responsible for the full-process design and development of medical device electronic systems, solve complex engineering problems with profound technical capabilities, promote product technological innovation and optimization, and ensure products comply with medical device industry standards and quality requirements.

Job Responsibilities

(I) Electronic System and Circuit Board Design

1. Lead the design of medical device electronic system solutions, including requirement analysis, architecture planning, and component selection. Combine with product clinical application scenarios to ensure the feasibility, reliability, and compliance of the solutions.

2. Be responsible for the full-process design of high-speed, high-precision printed circuit boards (PCBs), including schematic drawing, layout and routing, electromagnetic compatibility (EMC) optimization, thermal design, and design for manufacturability (DFM). Solve core problems such as signal integrity and power integrity in PCB design.

3. Participate in PCB sample production, soldering, debugging, and testing. Troubleshoot and resolve electronic defects in sample testing to ensure PCB performance meets product specifications.

(II) Signal Simulation and Verification

1. Use professional simulation tools (such as ADS, ANSYS, Cadence, etc.) to conduct signal simulation, power supply simulation, EMC simulation, etc. Predict and optimize the performance of electronic systems and circuits to improve product stability and anti-interference capability.

2. Formulate signal testing plans, build test platforms, complete the verification of key indicators such as signal integrity and timing characteristics, and generate simulation and test reports to provide data support for design iterations.

(III) FPGA Development and Programming

1. Proficiency in using Verilog/VHDL languages for FPGA program writing, simulation, debugging, and optimization to realize functions such as complex logic control, data acquisition, and processing.

2. Collaborate with embedded software engineers to complete FPGA and MCU/CPU interface development and data interaction debugging, ensuring efficient collaborative operation of hardware and software systems.

3. Maintain FPGA program versions, optimize code performance, and resolve logical vulnerabilities, timing constraints, and other issues in FPGA development.

(IV) Medical Device Product Compliance and Optimization

1. Be familiar with medical device industry standards (such as IEC60601.1, GB9706.1, etc.), ensure electronic design links comply with product registration, CE/FDA certification, and other compliance requirements. Participate in design reviews, failure mode and effects analysis (FMEA), and other work.

2. Track the operation status of electronic parts of mass-produced products, collect market feedback and fault data, carry out technical optimization and iterative upgrading to improve product performance and user experience.

3. Participate in supplier technical evaluation and management, coordinate with suppliers of electronic components, FPGA chips, etc., to ensure the quality and compatibility of purchased components, and control costs and delivery cycles.

(V) Team Collaboration and Technical Accumulation

1. Communicate efficiently with cross-functional teams such as mechanical design, software R&D, clinical verification, and quality control. Collaborate to promote product R&D projects and ensure projects are delivered on schedule.

2. Keep abreast of cutting-edge trends in electronic technology and the medical device industry, introduce new technologies and solutions, promote product technological innovation, and form technical accumulation and patent layout.

Qualifications

(I) Education and Major

Bachelor's degree or above in Electronic Engineering, Electrical Engineering and Automation, Microelectronics, Communication Engineering, or related majors.

(II) Work Experience

1. 5-10 years of relevant work experience in electronic engineering design. Candidates with medical device (such as diagnostic equipment, therapeutic equipment, monitoring equipment, etc.) electronic design background are preferred. Familiar with medical device R&D processes and compliance requirements.

2. Have full-process project experience of medical device electronic systems from solution design to mass production. Able to independently lead complex PCB and FPGA development projects.

(III) Core Skills

1. Proficiency in PCB design tools (such as Cadence Allegro, PADS, Altium Designer, etc.). Have practical experience in high-speed PCB design, EMC design, and thermal design. Able to independently solve complex problems in PCB design.

2. Possess profound signal simulation capabilities. Skilled in using simulation tools such as ADS, ANSYS, Sigrity, etc. Good at signal integrity, power integrity, EMC simulation, and optimization.

3. Proficiency in FPGA programming, master Verilog/VHDL languages. Have capabilities in FPGA logical design, timing analysis, simulation, and debugging. Experience in developing mainstream FPGA chips such as Xilinx/Altera.

4. Familiar with the selection and application of electronic components. Understand the design principles of analog circuits, digital circuits, and power circuits. Possess solid circuit analysis and fault troubleshooting capabilities.

5. Familiar with medical device industry standards (ISO 13485, GB9706.1, etc.). Able to ensure design links comply with compliance requirements. 

(IV) Comprehensive Qualities

1. Excellent communication and coordination skills. Able to efficiently interface with cross-functional teams, clearly express technical viewpoints, and promote project collaboration.  good speaking and writing in English.

2. Strong innovative thinking and problem-solving capabilities. Able to quickly respond to technical problems in R&D and propose reasonable optimization solutions.

3. Rigorous and responsible work attitude. Good documentation skills, able to standardize the output of technical documents such as design plans, simulation reports, and test reports.

4. Good team spirit, willing to share technology. Able to work under certain project pressure with strong execution.
 

How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
Indicate if this role is an office/field/onsite role.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.