Our client is a global medical device group.
Job Responsibilities:
- Responsible for the trial production process verification and mass production introduction during the transfer of domestic production lines.
- Optimize processes and manage production transfers based on product characteristics and develop process documentation including SOPs drawings process flowcharts etc.
- Handle technical process equipment and tooling issues during production and analyze and improve significant production problems.
- Assist with the procurement transfer and acceptance of production equipment and tooling.
- Regularly prepare process reports and reports to the group company.
- Complete other tasks assigned by superior leaders.
Job Requirements:
- Good verbal and written communication skills in both Chinese and English.
- Minimum diploma qualification or higher in mechanical automation materials engineering electronic engineering precision mechanics or other related fields.
- Proficient in using office software.
- Over 2 years of work experience; experience in a medical device company is preferred.
- Able to travel to China for short-term business trips for work reporting and training.