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AbbVie

Production Operator

Posted 3 Days Ago
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Hybrid
Dublin, IRL
Entry level
Hybrid
Dublin, IRL
Entry level
Operates pharmaceutical production equipment and completes manufacturing activities according to schedules, batch documentation, GMP standards, SOPs, and safety requirements. Prepares work areas and materials, performs in-process testing, investigates deviations, maintains quality records, and supports equipment changeovers and production targets. Equipment may include mills, granulators, blenders, tablet presses, coating systems, inspection machines, dispensing equipment, and encapsulation machinery.
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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

We are looking for a Production Operator to join AbbVie North Dublin supporting our production line.

Responsibilities include:

  • Following Quality Assessment requirements, GMP standards, and all applicable SOPs for equipment, plant operations, and production processes.
  • Carrying out production activities according to the schedule, manufacture order, and work instructions.
  • Preparing the work area by checking schedule accuracy, workplace readiness, and materials, including codes, lot numbers, expiry dates, and FIFO compliance.
  • Completing preparatory, process, and post-production tasks, including batch documentation, product identification, and sealing containers.
  • Operating assigned equipment such as mills, granulation, blending, tabletting, coating, inspection, dispensing, and encapsulation machinery.
  • Meeting OEE targets for cycle times and changeover times across all processes.
  • Completing Master Batch Paperwork accurately and in step with production progress.
  • Performing in-process testing, investigate deviations, notify supervisors when needed, and complete quality control documentation.
  • Following safety regulations, report incidents or concerns, and contribute to a safe and clean workplace.,
  • Maintaining good hygiene, professional conduct, and a commitment to continuous improvement.

    Qualifications

     

    • A Leaving Certificate or equivalent is required.
    • Knowledge/Interest in process Equipment and manufacturing.
    • MS Word, MS Excel, Outlook.                   
    • Good communication skills and good problem-solving skills.

    Additional Information

    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

    AbbVie Dublin, Dublin, IRL Office

    Dublin, Dublin, Ireland

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