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.
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.
This role will require shift work.
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