Task
1. Process validations, include IQ / OQ / PQ, in charge of acceptance of new equipment and its commissioning;
2. Process improvement / process and production equipment re-validation /the process parameters optimization.
3. Production BoM creation and maintenance.
4. Product / production work instruction creation and maintenance.
5. Participate quality improvement, improve manufacturing techniques;
6. Interpret customer drawing and technical requirements, making internal standard;
7. Lead the trial run and pilot run until mass production;
8. Other tasks assigned by manager

Skill and experience
1. Have 3 years PE / SQE or similar role working experience in foreign company is preferred, have flexible packaging industrial experience is plus
2. Must be good at Excel
3. Familiar with Minitab and Microsoft Power tools will be plus
4. Familiar with CAD system, and be good at the jigs designing.
5. Good English, include reading, writing and speaking.
6. Familiar with medical packaging industrial standards, regulations, especially ISO 11607.X and EN 868.X will be plus
7. Basic statistic knowledge, be good at DOE, Cpk, SPC etc data analysis.