Device Technician

Desired Skills: Manufacturing,GMP,Equipment

PE Global is currently recruiting for a Device Technician for a leading multi-national pharmaceutical client based in Sligo.

This is an initial 6-month contract working a shift pattern: Days initially this department also has an evening and night shift so flexibility to move to shift would be preferable. Shift info: Evening @ 16.7% – 16:00 – 00:00 (Friday finish at 23:00) and night @ 27% – 00:00 – 08:00 (Friday finish at 07:00).

Position 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 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 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.

Requirements:

• Secondary School Leaving Cert, or equivalent
• Exposure to pharmaceutical manufacturing equipment or equivalent 1 years experience
• Basic Microsoft Excel and Word skills
• EBR and TrackWise knowledge desirable
• May need to undergo a yearly test for 20/20 vision and colour-blindness

Interested candidates should submit an updated CV.

Please click the link below to apply, alternatively send an up-to-date CV to sean.molloy@peglobal.net

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland****