1. Responsible for V5 volumetric pump project performance testing. Draft a test protocol and report, allocate personnel resource, equipment resource to perform test task, and collect the test result and conclusion.2. Responsible for V5 volumetric pump and syringe pump production line validation. Draft validation protocol and report, cooperate with multiple departments perform production line validation, collect product assemble process problem and feedback it to PE.3. Reference to IEC 60601-2-24, draft flow rate analysis Excel sheet. It could exhibition instantaneous flow rate chart, cumulate flow rate chart, trumpet chart.4. Design performance testing room renovation layout CAD drawing. Design testing clamp angular surveying fixture.

1.Lead new product introduction to production, Responsible for development new product process routing and definite key and special process, develop process specification and engineering document. 2.Process technology support and improvement, responsible for machining, polishing, ultrasonic cleaning, laser marking, packaging process. Simplify laser marking process operation and shrink routing time.3.Process validation(IQ/OQ/PQ): I was complete the work IQ for Heat Oven, special process validation OQPQ for Flexible Drill Heat treatment, special process validation OQPQ for Chondrofix product assemble step.4. As a new project member, I give assistance to CFDA audit for new project , responsible for product process content statement. These project contains hip surgical instruments product, knee surgical instruments product, Trauma implant product.5. I was learned some quality control tools and management methods at work, such as 8D, PPAP, MSA,FMEA,SPC.