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Device technician

Sligo
Pe Global
Technician
Posted: 19h ago
Offer description

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 @ (Friday finish at 23:00) and night @ (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 ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland**** Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. Skills: Manufacturing GMP Equipment

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