Are you working in medical device quality and feel that it is time for a change? How do you feel about flexible working, stylish workspaces, great benefits and exciting products? Tempting enough to read on?
As the Quality Manager (Systems) you will have overall accountability for the Quality Management System.
Along with the flexible working, attractive benefits and great workplace, you as the Quality Manager, will be working for a world leader in research and have the opportunity to be part of a company that produces some fantastic diagnostic products .
Ideally we would like you to possess IVDR experience, worked to ISO 13485, US FDA 21 CFR 820 standards and having a Lead Auditor qualification would be desirable.
If you have a mixture of the skills required then please do get in contact and we can discuss further.