Senior Regulatory Affairs Specialist
Dozee
- Experience
- 5+ yrs
- Location
- Bangalore, Karnataka, India
- Job type
- Full-time
Required skills
- Q-Submission (Q-Sub)
- 510(k)
- Software as a Medical Device (SaMD)
- FDA
- EU MDR
- EU MDD
- EU AI Act
- ISO 13485
- CE Marking
- Microsoft?
About the role
5+ years of regulatory affairs experience, preferably in medical devices and SaMD; bachelor's degree; FDA Class I/II device submissions; EU MDR, notified body, ISO 13485, and digital health regulatory expertise.
About Dozee
AI-powered contactless remote patient monitoring and early-warning systems.
This page is fully interactive when JavaScript is enabled. Please enable JavaScript to apply or browse related roles.