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.

Pharmaceutical Research & Development

AbbVie pharmaceuticals combines advanced science with expertise to make strides in drug and treatment discovery, making a remarkable impact on people's lives

Job Description

We are now hiring a Device Technician to join our team in Abbvie Ballytivnan, Sligo. Here, you will work as a team member in production/operations areas in line with all safety, regulatory and organizational requirements, preparing equipment, work areas and materials and ensuring/verifying readiness of manufacturing operations.

A snapshot of your key responsibilities:

• Preparation and operation of moulding and ancillary equipment. ·
• Preparation and operation of automated assembly and ancillary equipment.
• Preparation and operation of Pad Printing and ancillary equipment.
• Preparation and operation of manual assembly and ancillary equipment.
• Troubleshooting day to day manufacturing issues which may impact on efficiencies, safety or quality.
• Completion of quality checks and achieving production quality targets.
• Supplying materials to the operations and equipment in a timely and safe manner.
• Responsible for labelling and packing of components and finished products.
• Operating of Coordinate measuring equipment, and other advanced metrology equipment.
• Operate fully automated and complex computer-controlled systems, including robotic and vision system technology.
• Participate in divisional project team for New Product Introduction and Improvement Projects.
• Resetting equipment as necessary to ensure the manufacture of quality components.
• Team coordination to maximize the effectiveness of all the team members.
• Documentation of all activities in line with GMP requirements.
• Cross training within the team and training of new members.
• Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
• Execution of routine manufacturing documentation, commissioning and validation protocols on an ongoing basis.
• Ensuring compliance with the Quality, Regulatory, GMP requirements and adherence to all AbbVie policies and relevant legislation.
• Execute manual assembly and visual inspection as required.

What you will need:

• A minimum 1-year experience in a similar role in a regulated manufacturing environment
• 3rd level qualification is desired

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