Manufacturing Technician

AbbVie

Ireland, ITonsitePosted Jun 25, 2026
Posting intelligenceActively listedReposted 5×, possible evergreen/ghost posting

Skills

aseptic-manufacturingcleanroom-operationsgmp-compliancebatch-documentationequipment-maintenanceenvironmental-monitoringcompoundingfilling-and-cappingautoclave-operationsterile-manufacturingquality-assurance

About the role

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

Job Description

We are now recruiting for Manufacturing Technicians to join our diverse Biologics team in Westport, on a fixed-term contract basis. As our newest technician, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding, filling and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring.

You will ensure the continued success of our business unit by taking ownership of duties such as compounding, filling, and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring.

PLEASE NOTE: The following role is a 12 hour monthly rotational shift pattern, covering days, nights, weekdays and weekends.

Responsibilities:

Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system

Perform activities associated with the compounding, filling and capping of an aseptic process.

Prepare components and equipment for processing into a Grade A environment.

Accurately completing documentation on time, accurately and legibly.

Keeping the Manufacturing area tidy and clean.

Review and update documentation as requested by the Production Manager

Participating in root cause analysis and problem-solving.

Completing compliant investigations and environmental excursions.

Adhering to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.

Follow gowning procedures on entry to areas

Report any machine issues to the Production Manager and the maintenance department.

Set-up, clean and maintain equipment

Transfer of waste material out of the cleanroom areas

Perform environmental monitoring

Participate in aseptic process simulations

Adhere to and support all EHS & E standards, procedures, and policies.

Qualifications

Leaving cert or equivalent qualification required.

2-3 Years working in a manufacturing environment, preferably Aseptic/Sterile Manufacturing.

Experience working in a cleanroom environment.

Third Level qualification in science or engineering discipline is an advantage but not essential.

Ability to build strong relationships and work within cross-functional teams.

Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.

Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.

Additional Information

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:

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