Quality Assurance Specialist
£20-30 per hour
3 Month Contract
We are searching for an experienced Medical Device professional who is experienced in Quality Assurance / Quality Engineering with excellent knowledge in implementing and improving quality management systems and working to ISO 13485 and ISO 9001.
This project is focused on enhancing the quality management system as per FDA 21 CFR 820 and updating with the latest versions of ISO 13485 and ISO 9001.
Duties and Responsibilities:
" Conduct a gap analysis on the QMS to identify gaps, evaluate and remediate to improve and maintain compliance.
" Take time to revise and re-write the SOPs.
" Create lean compliant systems.
" Perform audits on paperwork.
" Hands-on Quality Management System experience within the medical device. industry and within a manufacturing environment.
" Knowledge of ISO 13485 and FDA quality systems.
" Experience within a Medical Device Manufacturing environment.
If you have the relevant experience within Medical Devices and are interested, please send apply with your CV asap with interviews available at short notice.
Please send your CV and contact James Powell of TXM Recruit.
("quality assurance" OR qa OR "quality management system" OR QMS OR "iso 13485" OR FDA)
TXM Recruit is an equal opportunities employer. If you have any specific requirements or require assistance or reasonable adjustments to be made for you during the selection process due to disability or long-term health condition, we will do our best to assist you.