MANUFACTURING PROCESS ENGINEER – TUBE
GE HealthCare View all jobs
- Beijing
- Permanent
- Full-time
- Support new CT, MI & Xray tube production line setup.
- Lead to drive continuous quality improvement initiatives, analyze production data to pinpoint root causes of defects and develop corrective actions.
- Lead or support the setup, installation, calibration, and qualification (IQ/OQ/PQ) of new equipment and tooling.
- Perform routine and preventive maintenance of production line equipment to ensure maximum uptime and performance.
- Collaborate with cross‑functional teams to verify equipment functionality against specifications and regulatory requirements.
- Identify opportunities for process improvements and implement solutions to increase efficiency, yield, and repeatability.
- Provide technical support during production runs, troubleshooting issues related to equipment, processes, or materials.
- Maintain accurate documentation of maintenance activities, validation protocols, process changes, and quality records.
- Train and guide production technicians on proper equipment handling, standard operating procedures, and safety practices.
- Stay up to date with industry trends, emerging technologies, and best practices in electromechanical and vacuum systems relevant to CT, MI & Xray tube manufacturing.
- 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
- Support compliance/closure of Regulatory and Quality requirements before/after completing Design Outputs/Program Deliverables.
- Bachelor or above in Automation/ Electrical/ Electronics/ Electrovacuum Engineering or equivalent.
- Solid knowledge of CT, MI & Xray tube technology is preferred.
- Minimum 3 years of experience in manufacturing/design engineering, preferably in high‑precision medical device or electron tube production.
- Hands‑on experience with equipment installation, commissioning, and qualification processes.
- Strong problem‑solving skills with a data‑driven approach to process and quality improvement.
- Familiarity with quality management systems (e.g., ISO 13485, ISO 9001) and regulatory standards applicable to medical device manufacturing.
- Good communication skills in English (both written and spoken).
- Ability to work independently and as part of a multidisciplinary team in a fast‑paced environment.
- Proactive mindset with excellence problem solving oriented skills.
- Experience in lean manufacturing or Six Sigma methodologies is advantageous.
- Capable of managing multiple priorities while maintaining attention to detail.
- Demonstrated project leadership and influencing skills