Abbott Analyst II, Labeling and UDI in Plymouth, Minnesota

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.

We are seeking an experienced, high caliber Analyst II -- Labeling & UDI Systems who will be responsible for implementing and maintaining the effectiveness of Quality System (QS) and Production applications supporting Labeling and Unique Device Identifier (UDI). Analyst II will provide support for medium and large systems projects and initiatives.

Impact this role will have on Abbott

  • Evaluate business processes and applications for effectiveness.

  • Identify user needs and requirements.

  • Partner to translate user requirements into system requirements.

  • Assist with user application testing (UAT) and verification activities.

  • Analyze business results, discrepancies, and deliver solutions.

  • Correlate data and utilize sound analysis skills to determine capacity and limitations.

  • Maintain accurate data, and documentation.

  • Employ sound project management methodologies to deliver projects.

  • Communicate complex concepts in a manner understood by broad audiences.

  • Manage multiple concurrent deadlines.

  • Lead or support activities associated with medium/large system projects or initiatives with a labeling and/or UDI impact.

  • Facilitate review and approval of the project plans and deliverables.

  • Maintain knowledge of external requirements and new developments in database functionality and technologies.

  • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

  • Performs other related duties and responsibilities, on occasion, as assigned.

Your Experience (s), education and knowledge will further expand Abbott’s marketplace success:

  • Requires a Bachelor’s degree and a minimum of 1 to 4 years’ experience working with product labeling, quality systems and/or regulatory.

  • Proven ability to learn new software applications quickly.

  • Experience in Product Data Management (PDM), Manufacturing Execution System (MES), Enterprise Resource Planning (ERP), or SAP systems preferred.

  • Experience in Medical Device and/or a regulated environment preferred.

  • Advanced MS Excel skills and experience with other MS Office Software (MS Word, PowerPoint, MS Project).

  • Ability to work in a highly matrixed, fast-paced and geographically diverse business environment.

  • Ability to leverage and/or engage others to accomplish projects.

  • Excellent verbal and written communications with ability to effectively communicate at multiple levels in the organization.

  • Proven ability to multitask, prioritize and meet deadlines.

  • Exceptional organizational and follow-up skills, and attention to detail.

  • Ability to travel approximately 15%, including internationally.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email