Quality Inspector - Fixed Contract
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About the Company:
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My client is one of Ireland's leading companies in Medical Device Engineering, and they currently have an opportunity for a talented Quality Inspector to join their team.
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About the Position:
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This client is currently recruiting for a full-time Quality Inspector Documentation Control position (Specific Purpose contract for Maternity Leave Cover).
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Key Responsibilities:
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1. Approves incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials.
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2. Routine Final QA Product Inspections of finished parts in production by confirming specifications; conducting visual and measurement tests; communicating any non-conformances to Production Manager & Quality Dept.
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3. Routine Environmental Monitoring; pressure differential readings, Particulate Monitoring, Microbial Monitoring.
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4. Document inspection results by completing reports and logs; inputting data into quality database.
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5. Problem solving and continuous improvement investigations.
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6. Perform internal audits as required.
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7. Review and update QA Documentation.
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8. To provide assistance and support to the Quality Engineering and Operations function.
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9. Drive continuous improvement and best practices in QMS Right First Time.
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10. Maintains safe and healthy work environment by following standards and procedures; complying with legal regulations.
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11. Updates job knowledge by participating in educational opportunities.
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12. Ensure compliance to all applicable regulatory standards and cGMP procedures and practices.
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13. Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position.
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14. Review documentation for completeness.
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15. Responsible for scanning, filing, backing up and archiving quality documentation to maintain Arroteks quality management system.
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16. Maintain and control all external supplied documentation which may affect product realisation.
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Experience/Requirements:
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Leaving Cert plus minimum 3-year Medical Device assembly experience.
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Proficient computer skills.
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Understand general principles of EN ISO 13485 & FDA 21 CFR 820.
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Competent in Inspection method and reading drawings and specifications.
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Decision making ability coupled with the ability to work on one's own initiative and with minimum supervision is required, and ability to multitask and prioritise.
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Good interpersonal skills and organisational skills.
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Excellent attention to detail.
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Documentation skills.
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Competent in inspection methods and reading drawing and specifications.
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Understand the principles of product/parts and FIFO.
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Communicates any concerns about work process regarding environment impact, health or safety issues to their manager.
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Forklift Licence would be an advantage.
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Remuneration Package:
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A competitive package is available including generous salary and benefits.