Opening At Israel For QA & Regulatory Affairs, Project Manager
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| Opening At Israil For QA & Regulatory Affairs, Project Manager |
(Location - center, and north)
At least 3 years experience with maintaining a quality system in a medical device/pharmaceutical industry
At least 2 years experience and knowledge in medical device
regulation (CE and FDA at least)
Experience in writing and maintain DHF related documents Experience in writing and maintaining design controls and risk
management processes
Experience in writing and implementing Quality Procedures Experience in quality-related processes such as CAPAS, MRB/
NCR, in-process tests, and final release
Participation in regulatory audits
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