First or second degree in QA-engineering or equivalent .
Deep medical device standards knowledge and familiarity with ISO quality management systems. 
Fluent spoken and written English
Experience as a QA manager in a medical device manufacturer.
Regulatory support for at least two clinical trials.
Several medical device submissions to regulatory authorities (FDA, Notified Bodies, Health Canada, etc.)
*נא לציין ציפיות שכר, פניות ללא ציפיות לא תיעננה*

מיקום המשרה: באר שבע וצפון הנגב, רמלה לוד ושוהם

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פקס: 037608909