Company: Neuralink
Location: Fremont, CA, United States
Type: Full-time | Regulatory Affairs
About the Role
Neuralink is seeking a Senior Regulatory Affairs Manager to lead FDA regulatory strategy for innovative neurotechnology medical devices, including 510(k) and PMA pathways.
Requirements
- 8+ years in medical device regulatory affairs
- Class III device experience strongly preferred
- Deep knowledge of FDA submission processes
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