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Labeling Project Manager

Abbott

Plymouth, MNJob$61–123K/yrSeen 2w agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$61–123K/yr
Location
Plymouth, MN
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Abbott seeks a Labeling Project Manager at its Plymouth, MN site to lead labeling and UAL projects, develop schedules, manage master data, ensure regulatory compliance, and collaborate across functions, leveraging program management skills and strong communication.

Skills & qualifications

RequiredNice to have

Skills

Program Management MethodologiesOrganizational SkillsProblem SolvingCommunicationSchedule DevelopmentDocument Management SystemsRisk MonitoringData AnalysisFDA and EU Regulations KnowledgeGS1 Standards KnowledgeISO Standards KnowledgeERP SystemsPLM SystemsSAPWindchillDatabase ManagementAnalytics SoftwareMicrosoft ExcelMicrosoft PowerPointMicrosoft WordMicrosoft Access

Qualifications

BA or BS Degree in Business Engineering Supply Chain Management Logistics or Operations Management or Equivalent CombinationProject Management CertificationFive Years Medical Device Industry ExperienceTwo Years Leading Large Scale Multi Functional Programs

Benefits

Medical Insurance
401(k) Match
Tuition Assistance

Full job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

The Opportunity

This position will work out of our Plymouth, MN location.

The Labeling Project Manager will be responsible for meeting business needs by supporting the Labeling and Universal Addendum Labeling (UAL) teams by leading/implementing projects, conducting analysis, developing managing master data, communicating with cross functional teams, and problem-solving various challenges. Top candidates will have demonstrated skills in utilizing program management methodologies, excellent organizational and problem-solving abilities, and exceptional communication skills.

What You’ll Work On

  • Develop, communicate, and drive detailed schedules and timelines for program deliverables across multiple organizational functions.

  • Create and manage labeling and UAL change processes within the document management systems.

  • Work cross-functionally to identify and resolve labeling and UAL inconsistencies to meet applicable requirements and project timelines.

  • Monitor for program risks and issues, and drive for resolution.

  • Ensure cross functional alignment on objectives and tasks.

  • Manage Labeling and UAL master data and workflow via internal IT systems.

  • Manages concurrent deadlines and meets deadlines for assigned work/tasks. • Analyze and interpret large data sets and identify methods of resolution.

  • Complies to world-wide Labeling regulations and cross-functional business requirements.

  • Comply with company initiatives in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), FDA & world-wide regulations, business requirements, company policies and operating procedures.

Required Qualifications

  • BA or BS degree in Business, Engineering, Supply Chain Management and/or Logistics, or Operations Management or equivalent combination of education and work experience.

  • Project management certifications preferred.

  • Minimum 5 years medical device industry experience preferred.

  • 2+ years of successfully leading large-scale, multi-functional programs preferred.

  • Ability to manage projects and drive them to completion with attention to detail.

  • Requires ability to be innovative, resourceful, and work with minimal direction. • Knowledge of FDA & EU regulations, GS1 and ISO standards.

  • Strong written and verbal communication, at all organizational levels.

  • Ability to work within a team and as a leader in a fast-paced, changing environment.

  • Experience working in medical device industry with focuses on regulatory compliance, quality systems, labeling, or UDI preferred.

  • Experience working with ERP and/or PLM systems preferred. Preferably SAP and/or Windchill.

  • Database management and/or analytics software knowledge preferred.

  • Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.

  • Skilled in Microsoft Office specifically Excel, PowerPoint, Word, and Access.

Apply Now (https://www.jobs.abbott/us/en)

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott , and on Twitter @AbbottNews.

The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.

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 [email protected]

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