About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
Your role:
- Support QMS programs, e.g. Document Based QMS Project, Sunrise FDA readiness, etc
- Support the document control and record control, maintain, upgrade, and control of electronic copy or hard copy of standard, procedure, instruction, and record
- Support the localization, optimization, and simplification of PEPF procedure/work instruction/Template
- Support the DIM system phase-out and transition to Windchill
- Support to set up the training plan for local employee orientation, transfer/refresh training plan, and monitor the execution and updating follow-up
- Support to maintain QMS document training matrix,
- Assist the internal and external audit and audit finding/recommendation follow-up
- Other work is arranged by the line manager
You're the right fit if:
- Currently pursuing a bachelor’s degree or above, major in quality/science and engineering-related disciplines is preferred
- Native Chinese speaker and workable English (CET 4) at least
- Available to work 4-5 days per week, with a minimum internship duration of 4 months, 6 to 12 months would be preferable