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Responsibilities: 1. Manage new project/products development with APQP planning methodology, follow project schedules on time and cost within budget ; Obtain desired deliverables in different project stage and handed over correctly 2. Manager engineering change and release ECO internally and handed over correctly 3. Carry out process validation under validation protocols under product manufacturability & process feasibility; Put together open issues and make reaction plans by trouble-shooting. 4. Improve and optimize current production process with continuous improvements , such as by Improving production efficiency through problem solving and optimization 5. Capable to make PFMEA ,Flow Chart , working instructions and train operators. 6. Assisting other tasks that will be assigned by project manager or engineer manager. Requirements 1. College degree or above with professional mechanical or pharma background. 2. 5 years minimum project development or process development with automotive or medical production lines; Strong technical knowledge is ideal 3. Fluent in written English, good oral English is preferred. 4. Excellent communication skills and coordination skills on all levels, willing to take challenge 5. Willing to take challenge, obedient, responsible , reliable , careful and proactive with honest 6. Excellent Solid Works & AutoCAD skills, minimum 1 years 7. Proficient with Microsoft office software; PPT, WORD, EXCEL, etc 8. Experiences of multiple process validation such as ultrasonic welding, over moulding, etc. 9. Experiences in Medical or Automotive or Life science is preferred.