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Avery Dennison · Longford, LD, Ireland

Production Operator

Longford, LD, IrelandFull-timeManufacturing & Production

Listed on Avery Dennison’s official careers site. Posted July 17, 2026. Check that it is still open and apply there.

Apply on Avery Dennison’s careers site →

Job description

About the role As a Production Operator at our Longford site, you will play a key role in manufacturing high-quality materials used in medical and healthcare applications worldwide. You will work in a clean, safety-focused environment where precision, teamwork, and accountability are essential to delivering products that make a real impact. Our facility operates on a two-shift rotation system.

Candidates must be available for both cycles

Morning Shift: 6:00 AM – 2:00 PM Afternoon Shift: 2:00 PM – 10:00 PM Our predictable two-shift rotation is planned well in advance, giving you the clarity you need to manage your personal commitments with ease. We also recognize and reward your flexibility through a dedicated shift premium system, which increases your earning potential based on the specific hours you work. Apart from the two-shift rotation, we offer a dedicated night shift from 10:00 PM to 6:00 AM with no rotation.

The dedicated shift premium system, which increases your earning potential based on the specific hours you work, applies to the night shift as well.

Key Responsibilities

Responsible for supporting the day-to-day operation, output, quality, and performance of the relevant production or packing line. Operate and monitor production activities, equipment uptime, and target outputs while ensuring all batch documentation and cGMP standards are met. Review and implement accurate Standard Operating Procedures (SOPs) and report any variances or deviations to the Supervisor. Maintain production and packing areas in a clean and orderly manner while complying with all safety-related procedures.

Actively participate in Lean programs with a focus on line efficiency, waste reduction, and regular housekeeping duties.

Qualifications

Leaving Certificate or equivalent qualification. Good written and oral communication skills. Must have a positive attitude, a strong work ethic, and demonstrated reliability. Must be capable of working individually or in a team environment. Previous experience in a regulated manufacturing environment (medical device, pharmaceutical,food or GMP) is highly desirable.

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