Pharma Production Operator: GMP & Quality

AbbVie Inc.; Dublin; On-site; EUR 32,000 - 45,000; Full time

Job summary

AbbVie North Dublin is seeking a Production Operator to join our manufacturing team on the Dublin campus. You will follow GMP, SOPs, and quality requirements to operate equipment across milling, granulation, blending, tabletting, coating and encapsulation processes.

You will prepare and monitor production schedules, ensure correct materials, perform in-process testing and document batch records, while maintaining safety, hygiene and a culture of continuous improvement.

Qualifications

• 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.

Responsibilities

• Follow Quality Assessment requirements, GMP standards, and SOPs for equipment, plant operations and production processes.
• Carry out production activities according to the schedule, manufacture order and work instructions.
• Prepare the work area by checking schedule accuracy, workplace readiness and materials (codes, lot numbers, expiry dates, FIFO).
• Complete preparatory, process and post-production tasks, including batch documentation and sealing containers.
• Operate equipment such as mills, granulation, blending, tabletting, coating, inspection, dispensing and encapsulation machinery.
• Meet OEE targets for cycle times and changeover times across processes.

Skills

Process equipment knowledge

Communication skills

Problem-solving

Education

Leaving Certificate or equivalent

Tools

MS Word

MS Excel

Outlook

Job description

AbbVie North Dublin is seeking a Production Operator to join our manufacturing team on the Dublin campus. You will follow GMP, SOPs, and quality requirements to operate equipment across milling, granulation, blending, tabletting, coating and encapsulation processes.

You will prepare and monitor production schedules, ensure correct materials, perform in-process testing and document batch records, while maintaining safety, hygiene and a culture of continuous improvement.