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 knowledge in remediation, non-conformance / CAPA investigations to work with a growing medical device & healthcare company.
Your role within the Quality Assurance team will be to play a key role in a remediation project.
Duties and Responsibilities:
" Investigate, analyse, remediate and close off on non-conformance / CAPA whilst adhering to the compliance of the quality management system.
" 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.
" Knowledge in the areas of CAPA and remediation.
" Desirable that you will be a qualified lead auditor.
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 "Regulatory affairs" OR "ce mark" OR "ce marking" OR "technical files" OR "design dossier" OR 93/42 OR mdd OR "iso 13485" OR gmp)
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.