Description
A Quality Control Technician is required for a global medical solutions company to carry out daily product quality assessment for raw materials and finished goods working to ISO 9001:2008 Good Manufacturing Practices.
The successful candidate will have experience working to GMP's in a manufacturing and production environment and be capable of undertaking the following responsibilities:
- Monitoring of all Quality Control related In process documentation
- Analysis of supplier Certification to establish conformance and acceptance
- Verify calibration of equipment in accordance with ISO 9001:2008
- Create and maintain legible and accurate records and verify records created by others.
- Use MRP systems, to accept and reject raw materials, to release or quarantine finished goods
- Manufacturing sign off, of all QC related In process documentation on completion
- Manage and maintain the documentation system to support the manufacturing process and record retention systems.
- Investigate non-conformances including root cause analysis and take necessary action in conjunction with manufacturing, QA, Engineering and maintenance functions.
- Through non-conformance, to raise reports against the appropriate function/supplier
- To liaise with the appropriate functions to establish containment and disposition of non-conforming product
- Final Dock Audit of Finished Goods
- Creation of Certification - Analysis/Conformity as applicable
- Conduct data analysis through the use of SPC Charts and prepare reports from the data.
- Provide support to the manufacturing process, and engineering functions as necessary
Please apply through this advert or alternatively call Stef Walters to discuss in more detail