Quality Systems Engineer - Medical Devices

Kent
Negotiable
22 Jan 2013
19 Feb 2013
HA-12322788
Alice Miles
Engineering
Contract
Full Time

You shall ensure that all Quality System procedures are established under one system that implements the requirements of the FDA QSR, ISO 9001, ISO 13485, Medical Device Directive (MDD), and other national and international regulatory requirements, as may be established from time-to-time.

Ensures the CAPA and Internal audit systems are operating effectively and close out of corrective actions meets expected deadlines.

Key Skills:

ISO 13485, Medical Devices and CAPA systems

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