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Active
On-site
Minneapolis, MN, United States
Posted · 06.10.2016
SmartRecruiters (US)

# QARA Consultant

Deegit Inc

• Review and approval of the clinical workflow definitions for the subject devices
• Identification of the clinical hazards and associated harms for the subject devices
• Estimation of the severity and probability of occurrence for the clinically related hazardous situation
• Development of the clinical benefit statements for the subject device
• Understanding of device development in an FDA regulated environment
• Experience with ISO 14971 risk management activities
• Experience with the post market medical device support (complaint or risk analysis) All your information will be kept confidential according to EEO guidelines. Deegit Inc.

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