Full-Time
Quality Assurance and Regulatory Affairs Consultant
Deegit
IT staffing and consulting
No salary listed
Minneapolis, MN, USA
In Person
 Biology & Biotech (1) |
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- Understanding of device development in an FDA-regulated environment.
- Experience with ISO 14971 risk management activities.
- Experience with post-market medical-device support, including complaint or risk analysis.
- Review and approve the clinical workflow definitions for the subject devices.
- Identify clinical hazards and associated harms for the subject devices.
- Estimate the severity and probability of occurrence for clinically related hazardous situations.
- Develop clinical benefit statements for the subject device.
Deegit is an information technology staffing and consulting company. The company provides technical recruiting, contract staffing, project support, application services, cloud expertise, and workforce solutions. It serves businesses, technology organizations, hiring teams, consultants, and professionals across client industries. Its operating model centers on client engagements supported by recruiters, account managers, delivery teams, consultants, and corporate operations. Teams work across recruiting, software, cloud, data, quality assurance, account management, and client delivery. Work depends on specialist expertise, clear client coordination, practical delivery, and ongoing support across projects and operating teams.
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