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Operator, Manufacturing II - Evening Shift

Job in St. Joseph, Saint Joseph, Buchanan County, Missouri, 64506, USA
Listing for: Allergan
Full Time position
Listed on 2026-08-04
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production Associate / Production Line
Salary/Wage Range or Industry Benchmark: 22041 - 30307 USD Yearly USD 22041.00 30307.00 YEAR
Job Description & How to Apply Below
Location: St. Joseph

Company Description

About Abb Vie

Abb Vie'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 Abb Vie, please visit us at  Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube.

Job Description
  • Perform manual assembly and inspection of commodities and components to final product and GMP specifications.
  • Operate semi-automated manufacturing equipment to produce finished product.
  • Perform and document in-process quality checks on product and equipment in order to assure that batch record specifications are attained.
  • Move material to and from production lines as required to support efficient work flow.
  • Adhere to safety guidelines and follow proper PPE gowning practices.
  • Implementing and maintaining the effectiveness of the quality system.
  • Manual finishing of pharmaceuticals utilizing semi-automated and automated equipment.
  • Understand and support basic line changeover activities.
  • Verification of components and testing equipment necessary to assure that pharmaceuticals are labeled and packaged per specifications.
  • Assists with the set up and close out of work orders on production lines including beginning and end of lot line clearances.
  • Review and audit in process and completed work order packets for accurate and complete data entry, and proper documentation practices.
Qualifications
  • Leaving certificate (or equivalent)
  • 2+ Years of Experience
  • Knowledge of applicable regulations and standards affecting Pharmaceutical Products (e.g. CFR 210/211, cGMP) specifically
  • Previous related work experience in a pharmaceutical production environment, including knowledge of related cGMP requirements and procedures is preferred
Additional Information
  • Working Hours are 16:00-23:30 Mon - Thurs, Fri 12:00-18:00
  • 6 month contract initially.

Abb Vie 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.

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