Labeling Program Lead for Medical Devices

Abbott; Iowa (LA); On-site; USD 61,000 - 123,000; Full time

Benefits offered by this job

Free medical coverage

Retirement plan with high employer 1%

Tuition reimbursement

Education benefit

Job summary

Abbott in Plymouth, MN is seeking a Labeling Project Manager to support Labeling and UAL teams. You will lead projects, develop schedules, and manage master data while coordinating across regulatory, quality, and IT functions to ensure compliance and timely results.

Ideal candidates bring 5+ years in medical devices with strong project management, data analysis, and communication skills. The role emphasizes adherence to FDA/EU regulations and ERP/PLM systems like SAP or Windchill.

Qualifications

• BA/BS degree in Business, Engineering, Supply Chain Management or Operations Management.
• 5+ years in medical device industry preferred.
• 2+ years leading large-scale, multi-functional programs preferred.
• Knowledge of FDA & EU regulations, GS1 and ISO standards.

Responsibilities

• Develop, communicate, and drive detailed schedules for deliverables across functions.
• Create and manage labeling and UAL change processes in document systems.
• Coordinate cross-functional efforts to resolve labeling/UAL inconsistencies.
• Monitor program risks and drive timely resolutions.
• Manage labeling/UAL master data and workflow in IT systems.
• Analyze large data sets to identify resolutions and ensure compliance with regulations.

Skills

Project management

Cross-functional leadership

Regulatory knowledge

Data analysis

Excellent communication

Team leadership

Problem solving

Education

BA/BS in Business/Engineering/Supply Chain/Operations

Tools

SAP

Windchill

Job description

Abbott in Plymouth, MN is seeking a Labeling Project Manager to support Labeling and UAL teams. You will lead projects, develop schedules, and manage master data while coordinating across regulatory, quality, and IT functions to ensure compliance and timely results.

Ideal candidates bring 5+ years in medical devices with strong project management, data analysis, and communication skills. The role emphasizes adherence to FDA/EU regulations and ERP/PLM systems like SAP or Windchill.