Neuralink
Regulatory Engineer
$71K–$119K
Austin, Texas, United States · Full-time · Posted May 20, 2026
- Experience
- Preferred: 1+ years in regulatory submissions, technical documentation, or quality engineering for medical devices.
- Education
- Bachelor’s Degree or higher in an applicable engineering discipline.
About the job
Conduct regulatory affairs for Neuralink devices, including submissions, international regulatory interactions, and post-market compliance and reporting.
What you'll do
- Develop regulatory strategies and prepare pre-market submissions and post-approval reports.
- Partner with engineering and clinical teams to integrate regulatory requirements, evaluate changes, and plan approval pathways.
- Improve compliance tools and processes, communicate regulatory guidance, and support cross-functional problem-solving.
What they ask for
- Bachelor’s Degree or higher in an applicable engineering discipline.
- Strong technical writing and communication skills.
- Excellent collaboration and organizational skills; comfort working in a fast-moving, cross-functional environment.
Nice to have
- 1+ years of experience in medical-device regulatory submissions, technical documentation, or quality engineering.
- Experience with medical-device design, testing, risk management, preclinical/clinical studies, or class III/II devices.
Pay
$71,000 — $119,000 USD (base salary)
Tools
IDE, PMA, 510(k), ISO 14971
Model-written summary · the original posting is authoritative