An exciting new opportunity has arisen for a QA Assistant. My client is a world-leader in medical diagnostics, specialising in the research, development and manufacture of innovative products focused on Multiple Myeloma, and other immune disorders. My client is expanding rapidly into new territories over the coming years, and is entering a recruitment drive to reflect that market growth. In this role as a QA Assistant, you will be based in the client’s UK headquarters in state-of-the-art facilities, and your role will include:
·Management of specific NCRs and CAPAs across all areas of the Business from creation to closure.
·Administration of NCR and CAPAS on ERP system.
·To lead root cause analysis meetings, aid decision making and to be able to set corrections/corrective actions. Identify Preventive actions and improvements.
·Ensure NCR and CAPA are followed up in a timely manner and are regularly progressed with dept reps. To ensure out of date items are highlighted as a concern.
·To attend customer complaint meetings and provide suitable input to Quality Review Group and Risk Meetings following company procedures.
The ideal candidate for this position will be:
·From a science background
·Experience of Non -Conforming Product and Corrective Action systems.
·Excellent communication skills
·Excellent eye for detail
·Ability to follow processes
·Knowledge of ISO 13485 would be hugely beneficial.
In order to be considered for this role, candidates must be able to prove that they have full rights to work in the UK.