Main responsibilities:
- Maintain NMPA required labeling data, label templates and applicable Quality systems documentation
- Manage CMIIT required RoHS labeling projects
- Support global UDI sustaining activities
Required skills and abilities:
- Strong communication skills
- Demonstrated abilities to work cross-functionally
- Demonstrated abilities to run small scale projects
- Intermediate Excel Skills (sorting, filtering, and conditional formatting, using VLOOKUP, PivotTable, creating basic charts)
Preferred skills:
- Experience working in medical device industry
- Research, learn and understand medical devices regulations
- Experience with Quality systems principles as applicable to the medical device industry
- Experience with Product life cycle management (PLM) / Windchill, enterprise resource planning (ERP) / SAP, and labeling application systems
- English fluency
