Quality Inspector - Fixed Contract
About the Company:
{company} 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
This client is currently recruiting for a full-time Quality Inspector Documentation Control (Specific Purpose contract for Maternity Leave Cover).
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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.
* 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 realization.
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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 one's own initiative and with minimum supervision is required, and ability to multitask and prioritize.
* Good interpersonal skills and organizational 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.
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Remuneration Package
A competitive package is available including generous salary and benefits.