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Packaging Analyst Visual Inspection
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AbbVie

Packaging Analyst Visual Inspection

Onsite Kansas City, MO, United States Full Time Mid-Level
Posted a day ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.


Job Description

The Packaging Analyst plays a critical role in ensuring the effectiveness of packaging operations by training and qualifying Inspectors, updating SOPs and Work Instructions, performing periodic reviews in OneVault, creating and maintaining defect qualification sets, trending inspection data, and supporting investigations and process improvements.

Responsibilities:

  • Training/Qualification
    • Train and qualify Inspectors for Core 1 Products
    • Create and manage defect qualification sets
    • Trend batch data from inspection records
    • Generate and update controlled documents, procedures, and work instructions in OneVault
    • Initiate, document, and support change controls (Global Trackwise) and process updates
    • Complete and document investigations, CAPAs, non-conformances, root cause analysis, and system risk assessments
  • Administration/Meetings
    • Attend Tier and CAPA Investigation meetings with internal stakeholders
    • Support other duties as required

Qualifications

  • Knowledge of regulatory requirements in a pharmaceutical GxP environment
  • Minimum 3 years’ experience in a regulated environment
  • Preferred: Experience with S4 HANA, OneVault, Global Trackwise, MS Office

Additional Information

The deadline for applications for this role is the 20th March 2026

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Required Skills
  • Training/Qualification
  • Regulatory Requirements
  • GxP Environment
  • S4 HANA
  • OneVault
  • Global Trackwise
Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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