Labeling Specialist II

Abbott

Shanghai (VA)

On-site

USD 75,000 - 120,000

Full time

13 hours ago
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Job summary

Abbott in the United States seeks a labeling specialist to maintain NMPA labeling data, label templates and applicable Quality systems documentation. You will support CMIIT RoHS labeling projects and assist with global UDI sustaining activities.

The role requires strong communication, cross-functional collaboration, and the ability to run small scale labeling projects, with intermediate Excel capabilities. Experience in the medical device industry is preferred.

Qualifications

  • 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).

Responsibilities

  • Maintain NMPA required labeling data, label templates and applicable Quality systems documentation.
  • Manage CMIIT required RoHS labeling projects.
  • Support global UDI sustaining activities.

Skills

Strong communication
Cross-functional work
Small projects
Excel advanced

Tools

Windchill
SAP

Job description

  • Maintain NMPA required labeling data, label templates and applicable Quality systems documentation
  • Manage CMIIT required RoHS labeling projects
  • Support global UDI sustaining activities
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
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