Posted:
8/10/2026, 7:51:24 PM
Location(s):
Shanghai, China
Experience Level(s):
Junior ⋅ Mid Level ⋅ Senior
Field(s):
Legal & Compliance
Workplace Type:
On-site
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
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
Website: https://abbott.com/
Headquarter Location: Illinois City, Illinois, United States
Employee Count: 1001-5000
Year Founded: 1944
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Biotechnology ⋅ Emergency Medicine ⋅ Genetics ⋅ Health Care ⋅ Health Diagnostics ⋅ Manufacturing ⋅ Medical ⋅ Medical Device ⋅ Nutrition ⋅ Pharmaceutical
Visa Sponsorship: Sponsors work visas