Senior Medical Representative jobs at Ge Healthcare in China, Luyang District

1. Roles & Responsibilities

• Executing design visualization efforts with 3D CAD models and essential component and assembly details to explore multiple design options
• Developing innovative designs to meet all requirements for performance, reliability, cost, and manufacturability
• Developing engineering design concepts for components and electromechanical assemblies that have tough requirements for size, precision, reliability, and cost
• Leading quality engineering projects that provide imaginative solutions to engineering and customer issues
• Influencing cross-functional teams to implement quality actions
• Delivering improvements to customer focused metrics
• Validating product sub-system reliability performance

2. Qualification/Requirements

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
• Complete all planned Quality & Compliance training within the defined deadlines
• Identify and report any quality or compliance concerns and take immediate corrective action as required
• Support compliance/closure of Regulatory and Quality requirements before completing Design Outputs/Program Deliverables
• Participate in continuous improvement activities by identifying and appropriately escalating process and product quality gaps, providing solutions when possible

3. Desired Characteristics

• MS or above in Mechanical Engineering or equivalent (defined as 5 years relative engineering experience)
• 5+ years working experience in mechanical design
• Experience/knowledge of robotics and autonomous system design is preferred
• Good communication in English
• Experience of working in global team and familiar with manufacturing process

4. Inclusive & Diversity

5. Behavior Statement

6. Total Rewards Statement

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

Job Roles and Responsibilities

• Be responsible for Embedded software design for CT system

• Design, integration, verification and validation implementation by either special or common testing equipment off or inside

system, responsible for defining and executing validation plan

• Data Acquisition and / or control subsystem firmware design with compliance of GE product development process

• Responsible for ensuring the quality of his or her design

Job Requirements:

• No need to meet all requirements below, partly meet is ok for application

• Major in electrical engineering, computer engineering, automation, mechatronics or biomedical engineering, etc. Master degree or above is desired

• Experience in embedded system design with NIOS, Arm, DSP or other kinds of 32/16/8 bit MCU

• Experience in firmware coding with C/C++, RTOS experience of Vxworks, Nucleaus, eCOS or RT linux, basic understanding of version control tools such as ClearCase etc

• Sense in product life cycle, reliability and serviceability

• Experience & knowledge in Control Systems; Data Acquisition Systems, etc

• Basic knowledge in CAN, Ethernet, wireless communication

• Experience in FPGA design, VHDL or verilog language, Altera or Xilinx FPGA, FPGA design tools such as Quartus or ISE Foundation will be a plus

• Experience in Digital / analog circuit design, be familiar with multi layers PWB / PWA layout, knows either

one of these tools: Cadence / OrCAD / Protel, etc will be a plus

• Good Communications in written and spoken English

• Team player, self-motivated, embrace global culture

Inclusion and Diversity

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

Lead software architecture design for C-arm products, ensuring scalability, maintainability, and innovation.
Drive selection and implementation of key technical solutions, ensuring effective architecture execution.
Collaborate with cross-functional teams including product, image quality, system, EE, and ME to align architecture with system requirements.
Influence large cross-functional teams and drive technical alignment.
Drive product evolution with innovative design and high quality and affordable cost.
Stay current with industry trends and promote adoption of emerging technologies.
Identify team competency gaps and implement development plans to drive excellence.
Coach and mentor engineers to support technical growth.
Guide the development team in module design and implementation, enhancing technical capabilities.
Troubleshoot complex system-level issues and perform performance optimization.
Continuously improve software development processes and promote best engineering practices within the team.
Lead the creation and implementation of design guidelines.
Author and maintain architecture documentation, technical specifications, and design descriptions.
Drive innovative architecture by integrating AI, machine learning, and intelligent image analysis.
Evaluate AI feasibility in clinical scenarios and drive real-world applications in C-arm products.Bachelor’s degree or above in Computer Science, Software Engineering, Electronic Information, or related fields.
8+ years of experience in medical device software development, with 3+ years in software architecture
Proven ability in strategic planning and driving technical evolution.
Strong experience in object-oriented design, modular architecture, and system integration.
Proficient in C/C++ and Java, with experience in Linux platforms.
Familiar with IEC 62304, ISO 13485 and other medical software standards.
Excellent communication, collaboration, and project leadership skills.
Proficient in both Chinese and English technical communication.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

Roles and Responsibilities

• System Architecture & Design: Lead the development of system and architecture and design, including system-level requirements and interface specifications

• Integration & Performance: Oversee integration of subsystems to ensure optimal image quality, patient safety, and system reliability; Drive system-level performance analysis and trade-off studies.

• Technical Leadership: Serve as the technical point of contact for cross-functional teams including hardware, software, clinical applications, and regulatory affairs; Mentor junior engineers and contribute to technical reviews and design decisions; Lead risk assessments and failure mode analyses (FMEA) for system-level concerns.

• Lifecycle Management: Support product development from concept through commercialization and sustaining engineering; Lead system verification and validation planning and execution; Ensure compliance with medical device regulations (e.g., FDA, IEC 60601).

• Stakeholder Collaboration: Translate customer and clinical needs into system requirements and design inputs; Work closely with product management, marketing, and service teams to ensure product success; Interface with external partners and suppliers as needed.

Required Qualifications

• Bachelor’s or Master’s degree in Electrical Engineering, Biomedical Engineering, Physics, or related field (PhD preferred).

• 3+ years of experience in systems engineering, preferably in medical imaging or MRI.

• Strong understanding of MRI physics, system components, and clinical workflows.

• Proficient in the use of software tools for analysis and simulation.

• Experience with regulatory standards and design controls for medical devices.

• Excellent communication, analytical, and problem-solving skills.

Desired Characteristics

• Experience with MRI system modeling, simulation, or performance optimization tools.
• Familiarity with advanced imaging techniques (e.g., diffusion, spectroscopy, functional MRI).
• Hands-on experience with MRI hardware or software development.
• Knowledge of signal processing and image reconstruction algorithms.
• Experience working in Agile or hybrid development environments.
• Prior involvement in clinical trials or collaboration with radiologists and technologists.
• Strong background in risk management and safety-critical systems.
• Experience with international regulatory submissions (e.g., CE Mark, MDR).

Essential Responsibilities:

• Designing the embedded hardware for the medical system including:

• FPGA development: Architecture design, VHDL/Verilog programming, timing/control sequence analysis, simulation
• Analog/Digital circuits design: Embedded CPU and Peripheral selection, interface design, schematic design, PCB layout, debugging and testing
• High speed serial communication, signal integrity analysis

• Engaging in all phases of new product introduction, including concept, architecture, documentation, design, prototype, test, supplier interfaces, manufacturing introduction and service support

• Lead technical design review for concept solution, detail design and evaluation result with global team

• Perform electrical parts’ FMEA, reliability, manufacturability and serviceability analysis

• Keep track on new technology, methodology and design concept. Identifying and developing new opportunities to leverage Strategic Sourcing objectives and Common Technology initiatives

Qualifications / Requirements:

• BS or above in Electrical Engineering, communication engineering or equivalent experience

• 5 years engineering experience in Medical device, automation, instrumentation, or telecommunication industry

• Strong design capabilities in any of the following: FPGA (VHDL/Verilog), Circuit boards design, high speed digital design and mixed signal design, embedded system hardware design

• Skillful on electrical design and simulation tools like Cadence, Quartus, ModelSim, etc

• Fluent English communication

Desired Characteristics:

• Self-starter, energizing, results oriented, and able to multi-task
• Excellent teamwork, coordination and communication skills
• Ability to meet aggressive reliability, performance, cost, serviceability, and delivery targets
• Effective oral and written communication skills, global project experience will be plus.

• Demonstrated technical leadership capability in integration activities

Inclusion and Diversity

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

Description:

Roles & Responsibility:

Duties include (but are not limited to):

• Working across functions and team boundaries to define, design, and implement the next generation of products
• Providing domain expertise to serve as the main integrator between the hardware and software functions to deliver high quality systems
• Working with customers, marketing and field personnel to refine requirements which can be follow by the engineering teams
• Developing methods to quantify subsystem interactions and their effects on system feature and performance.
• Delivering and incorporating feedback results into new hardware, software, and service specifications

Quality Specific Goals:

1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position

2. Complete all planned Quality & Compliance training within the defined deadlines

3. Identify and report any quality or compliance concerns and take immediate corrective action as required

4. Support compliance/closure of Regulatory and Quality requirements before completing Design Outputs/Program Deliverables

5. Participate in continuous improvement activities by identifying and appropriately escalating process and product quality gaps, providing solutions when possible

Qualification/ Requirements:

1. Bachelor’s degree or above major in Biomedical Engineering, Computer Science, Electrical Engineering, or closely related discipline

2. Bachelor 6+ years, Master 4+ years working experience in R&D.

3. Broad exposure to HW/SW/Systems design, and good technical depth in one or more engineering disciplines (Electrical, Image Processing, Software, etc.)

4. Proven ability to develop timely and effective solutions for challenging design problems

5. Excellent teamwork, coordination and communication skills

:

1. Product design experience in medical devices, especially in Mobile C-arm, X-ray, CT, DSA product

2. Effective oral and written English communication skills, global project experience will be plus

3. Self-starter, energizing, results oriented, and able to multi-task

4. Demonstrated technical leadership capability in integration activities

Total Reward Statement

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support

Roles and Responsibilities:

Ensuring that the product development process abides to the Quality Management System, Phased Review Discipline, and regulatory needs of the applicable markets.

Executing project plans according to committed timelines and within regulatory and quality guidelines and processes, including coordination of all cross-functional tasks and deliverables to meet quality, deployment, performance, and productivity goals.

Developing project plans and driving execution of program milestones for Design, Development, Maintenance, or Manufacturing transfer programs.

Required Qualifications:

Bachelor's Degree within appropriate Engineering/Science discipline.

Minimum of 5 years of experience developing, leading, driving and commercializing new product introduction and/or product change projects/programs.

Minimum of 5 years of experience working with cross-functional teams demonstrating strong influencing and communication skills.

Inclusion and Diversity

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.