Senior Quality Specialist
Posted on Apr 16, 2019 by Anonymous
The Senior Quality Specialist will be maintain the compliance of Global Quality Standards against the changing device and IVD regulations; EU MDR, IVDR and associated legislation. You will also be coordinating management reviews, post market surveillance, DHF audits and independent design reviews.
Additional responsibilities will include supporting EU Medical Device complaints and day to day product quality; deviations, CAPA resolution, CMO management, change control, etc...
If you would like to apply for this opportunity then please send your CV or please call Craig on +(phone number removed)
STR Limited is acting as an Employment Business in relation to this vacancy