Senior Director, Regulatory Affairs - Product Development
Artivion, Inc.
- Experience
- 12+ yrs
- Location
- Kennesaw, Georgia, United States
- Job type
- Full-time
About the role
Bachelor's degree in science, engineering, life sciences or related field; 12+ years regulatory affairs or medical device experience with significant leadership, or 10+ years with master's; extensive experience with Class II/III devices and global regulatory submissions.
About Artivion, Inc.
Public medical-device and human-tissue company serving cardiac and vascular surgeons treating aortic disease.
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