Packaging Operator: cGMP, Safety & Quality Focus

AbbVie Inc.

Westport

On-site

EUR 32,000 - 46,000

Full time

44 hours ago
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Job summary

AbbVie in Ireland is seeking a dedicated operator to support core packaging lines and ensure adherence to safety, quality and cGMP standards. You will perform in-process checks, complete batch documentation and maintain a clean, compliant workstation on a daily basis.

The role requires adaptability, strong teamwork across functions, and a proactive mindset to participate in safety and quality initiatives while staying current with trainings and SOPs.

Qualifications

  • Adaptability to changing business needs and constraints.
  • Ability to build strong working relationships across functions.
  • Business-minded with focus on priorities and outcomes.
  • Proactive change management and agile response to change.
  • Clear written and verbal communication with shift teams.
  • Willingness to identify opportunities and implement simple solutions.
  • Strong analytical thinking to drive better decisions.
  • Customer-oriented approach prioritizing end-user requirements.

Responsibilities

  • Maintain AbbVie's Safety, Environmental and Quality goals and SOPs.
  • Operate TLM packing and semi-automated packing lines.
  • Perform in-process checks and complete batch documentation per cGMP.
  • Keep workstation clean, organized and compliant with procedures.
  • Stay current with cGMP and safety training via eLMS.
  • Engage in departmental safety, quality and improvement programs.
  • Carry out additional duties as assigned.

Skills

Adaptability
Build relationships
Business minded
Change management
Communication
Continuous improvement
Critical thinking
Customer orientated
Decision making
Innovation
Management under pressure
Excellence focused
Optimistic mindset
Open and authentic
Ownership mentality
Boundaryless mindset
Outside-in perspective

Job description

AbbVie in Ireland is seeking a dedicated operator to support core packaging lines and ensure adherence to safety, quality and cGMP standards. You will perform in-process checks, complete batch documentation and maintain a clean, compliant workstation on a daily basis.

The role requires adaptability, strong teamwork across functions, and a proactive mindset to participate in safety and quality initiatives while staying current with trainings and SOPs.

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