Neuralink is creating devices for a bi-directional interface with the brain to restore movement, sight, and revolutionize human interaction with the digital world
Job Summary
Neuralink is creating devices for a bi-directional interface with the brain to restore movement, sight, and revolutionize human interaction with the digital world.
The Quality Team focuses on exceeding regulatory requirements and industry best practices for safe and fast development of innovative technologies.
This role will support the maintenance, development, and scaling of processes, archiving, and compliance tracking, ensuring traceability, version control, and readiness for audits and submissions.
Matching Summary
Neuralink is creating devices for a bi-directional interface with the brain to restore movement, sight, and revolutionize human interaction with the digital world.
Salary
$21 – $35/Hr USD
Skills & Requirements
Must-have
Sustain and improve document control systems
Organize GxP files into a traceable system
Manage document lifecycles and workflows
Support regulatory filings and submissions
Proficiency with Google Suite and document management tools
Nice-to-have
Meticulous attention to detail
Exceptional organizational skills
Excellent verbal and written communication
Strong multitasking abilities
Working knowledge of regulatory terminology
Key Requirements
FDA regulations (e.g., 21 CFR Part 11, 21 CFR 58, 21 CFR 812)
GxP requirements
Bachelor's Degree in a relevant field (preferred)
Relevant experience in regulated environments (preferred)