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Device Technician

Our client a leader in the Pharmaceutical Industry is seeking Device Technicians to join their Sligo team. 12 month contract | Must be flexible to work shift .

 

Job Summary:

To 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

 

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 labeling 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 of 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.

·       Ability to work on own initiative.

·       Execute manual assembly and visual inspection as required.

 

Essential Requirements

·       Leaving Certificate or equivalent, desirable · or relevant work experience.

·       Working knowledge of: Microsoft Office Suite beneficial.

·       Minimum 1 year of experience in regulated manufacturing environment required.

 

 

 For a confidential discussion and more information on the role, please contact Emma Daly

emma.daly@collinsmcnicholas.ie

0861041202


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