Job Title
Advanced Manufacturing EngineerJob Description
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In this role, you have the opportunity to
To participate in working for high growth business that will help improve the lives of millions of men globally, while advancing Philips digital transformation journey as a global leader in Health Technology.
You are responsible for
- Quality Control and Improvement
- Ability to conduct root cause analysis; work out short/long term solution with functional team to
mitigate line interruption.
- Evaluate design change and supplier change request to identify potential impact to product quality.
- Support MQ and SQE to conduct incoming failure parts analysis.
- Take lead to analyze customer complaint and DEFOA, MOA, WOA, DOA.
- Work with quality team to fulfil QMS requirement and support TUV, NMPA, and FDA audit.
- Line Sustaining
- Responsible for welding process, define and optimize process specifications, train and qualify welders.
- Perform troubleshooting of welding related defects and welding quality issue from supplier
- Familiar with ASME and PED regulations, support the relevant audits.
- Update WI and DHR according to ECR from designer or PPC.
- Execute WI training and technical training to manufacturing team.
- Daily NC analysis, find root cause and drive improvement.
- Support equipment team to install, verify, maintain and repair production equipment.
- Support change controller to execute ECO in production on time and minimize the line interruption.
- Introduce new product / new process / new part in production.
- LEAN and Cost Reduction
- Continuously improve production efficiency by standardized work, line balance and automation project.
- Optimize production process and eliminate waste using lean method and tools.
- Organize and lead the lean activities and other improvement project.
- Equipment Trouble Shooting and Improvement
- Familiar with welding equipment, parameter setting and troubleshooting
- Identify opportunities to improve current equipment or create new equipment and work with R&D or
supplier to realize the requirement.
- Define the URS to guide new equipment purchasing and the equipment qualification.
- Define the gauge calibration requirement.
You are a part of
A progressive and energetic team that contributes directly to the growth of the business. You have a direct reporting line to the function manager.
To succeed in this role, you should have the following skills and experience
- B.S. or above in mechanical, or engineering related majors.
- 8 years of experience working in medical device manufacturing or finish medical device assembly.
- Familiar with NMPA, FDA Regulations and ISO13485 Quality System.
- Experience of Windchill and SAP.
- Knowledge and methodology of six sigma and Lean manufacturing.
- Knowledge of process verification and validation knowledge.