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Group Leader, Device

Posted on Sept. 16, 2025

  • Sligo, Ireland
  • 0 - 0 USD (yearly)
  • Full Time

Group Leader, Device

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Company Description


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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


Job Description


What you do, is what we need. Making a difference begins here. And takes all of us.

Welcome to AbbVie!
We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work.

Purpose:

We are seeking a new Device Group Leader to join the team in AbbVie Ballytivnan. The purpose of this role is to support the Operations Supervisor in moulding and Assembly areas, in line with all safety, regulatory and organisational requirements. Successful candidate will report directly into the Shift Supervisor.

What you will do:

  • Plan and communicate the daily production work load.
  • Attend Management and production related meetings when required and be involved in executing any actions required.
  • Coordinate the team to maximize the effectiveness of all the team members.
  • Work closely with the QA Team to ensure that all products are meeting the required standards at all times.
  • Promote a culture of quality among the team.
  • Complete Batch reviews on PI Sheets and applicable paperwork and ensure Batch Right First Time.
  • Troubleshooting day to day manufacturing issues which may impact on efficiencies, safety or quality.
  • Ensure completion of Line Clearances and Verification are done efficiently.
  • Coordinating Transport of Materials/Components from/to Warehouse.
  • Documentation of all activities in line with GMP requirements.

Qualifications


What you will need:

  • Minimum 2 years’ experience in a GMP environment is essential
  • 3rd level qualification in a related discipline is desirable
  • Experience working in a fast paced environment
  • Ability to work under your own initiative and to prioritise tasks

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


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