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Orion Group Life Sciences are currently recruiting a Device Technician on behalf of our Multinational Biopharmaceutical Client based in Sligo on an initial 6-Month contract with potential to extend.
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). Both eligible for OT/DT.
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 policies and relevant legislation.
* Ability to work on own initiative.
* Execute manual assembly and visual inspection as required.
Qualifications:
* Leaving Certificate or equivalent, desirable · or relevant work experience
* Working knowledge of: Microsoft Office Suite beneficial.
Desired Requirements
* 3rd level education.
Experience required:
Technical/Business Knowledge -Job Skills/Experience Required
* Minimum 1 year of experience in regulated manufacturing environment required.
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Contract
Job function
* Job function
Production, Science, and Manufacturing
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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