Quality Inspector – Documentation Control
This is a fixed-term contract to cover maternity leave.
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.
* Provide assistance and support to the Quality Engineering and Operations function.
* Drive continuous improvement and best practices in QMS “Right First Time”.
* Maintain a safe and healthy work environment by following standards and procedures; complying with legal regulations.
* Ensure compliance with all applicable regulatory standards and cGMP procedures and practices.
* Reviews documentation for completeness.
* Responsible for scanning, filing, backing up, and archiving quality documentation to maintain the quality management system.
* Maintain and control all externally supplied documentation which may affect product realization.
Requirements:
At least 1 year's experience as a Quality Inspector in Medical Devices.
Salary: Estimated salary range: €30,000 - €40,000 per annum based on location and industry standards.