Labeling Project Manager
Abbott · Plymouth, MN
RegulatoryFull-time$61k–$123kCompany career page
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Role summary
Abbott seeks a Labeling Project Manager for its Plymouth, Minnesota facility to oversee labeling and universal addendum labeling projects. The role involves managing cross-functional initiatives, regulatory compliance documentation, and master data systems while ensuring adherence to FDA and international standards.
What they're looking for
- Bachelor's degree in Business, Engineering, Supply Chain Management, Logistics, or Operations Management
- Minimum 5 years medical device industry experience preferred
- Project management certification preferred
- Knowledge of FDA, EU regulations, GS1, and ISO standards
- Experience with ERP or PLM systems, preferably SAP or Windchill
- Advanced proficiency in Microsoft Office, especially Excel and PowerPoint
- Strong analytical and data management skills with attention to detail
What you'll be doing
- Develop and communicate detailed schedules and timelines for labeling deliverables across organizational functions
- Create and manage labeling change processes within document management systems
- Identify and resolve labeling inconsistencies to meet regulatory and project requirements
- Monitor program risks and issues, driving resolution and cross-functional alignment
- Manage labeling master data and workflow via internal IT systems while ensuring regulatory compliance
Privacy & handoff
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