Quality Inspector- Fixed Contract

4 days ago

Sligo, Ireland Brightwater Full time

Quality Inspector- Fixed Contract About the Company 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. About the Position This client is currently recruiting for full-time Quality Inspector Documentation Control (Specific Purpose contract for Maternity Leave Cover). Key Responsibilities Approves incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials. 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. Routine Environmental Monitoring; pressure differential readings, Particulate Monitoring, Microbial Monitoring. Document inspection results by completing reports and logs; inputting data into quality database. Problem solving and continuous improvement investigations. Perform internal audits as required. Review and update QA Documentation. To provide assistance and support to the Quality Engineering and Operations function. Drive continuous improvement and best practices in QMS Right First Time. Maintains safe and healthy work environment by following standards and procedures; complying with legal regulations. Updates job knowledge by participating in educational opportunities. Ensure compliance to all applicable regulatory standards and cGMP procedures and practices. 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. Review documentation for completeness. Responsible for scanning, filing, backing up and archiving quality documentation to maintain Arroteks quality management system. Maintain and control all external supplied documentation which may affect product realisation. 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. Experience/Requirements Leaving Cert plus minimum 3-year Medical Device assembly experience. Proficient computer skills. Understand general principles of EN ISO 13485 & FDA 21 CFR 820. Competent in Inspection method and reading drawings and specifications. Decision making ability coupled with the ability to work on ones own initiative and with minimum supervision is required, and ability to multitask and prioritise. Good interpersonal skills and organisational skills. Excellent attention to detail. Documentation skills. Competent in inspection methods and reading drawing and specifications. Understand the principles of product/parts and FIFO. Communicates any concerns about work process regarding environment impact, health or safety issues to their manager. Forklift Licence would be an advantage. Remuneration Package A competitive package is available including generous salary and benefits. Contact Please contacton oror simply click the apply button. To view all live jobs with Brightwater and market insights, please visit our website:

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