Document Control Specialist at Neuralink

Austin, Texas, United States -

Full Time

Start Date

Immediate

Expiry Date

15 May, 26

Salary

35.0

Posted On

14 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Organization Skills, Document Control, Process Maintenance, Archiving, Compliance Tracking, Traceability, Version Control, Audit Readiness, FDA Regulations, GxP Requirements, SOP Development, Document Lifecycle Management, eTMF Management, Attention To Detail, Communication Skills, Multitasking

Industry

Biotechnology Research

Description

About Neuralink: We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world. Team Description: Join the Quality Team at Neuralink, a group of dedicated professionals building and sustaining world-class quality and compliance frameworks from the group up. The Quality team focuses on exceeding regulatory requirements and industry best practices to enable safe and fast development of Neuralink’s innovative technologies. Job Description and Responsibilities: Neuralink is seeking a Document Control Specialist with strong organization skills to support document control-related activities company-wide. This role will serve as a foundational resource for organizing and managing critical documentation across the preclinical, manufacturing, engineering, quality, and regulatory departments. This position will support the maintenance, development, and scaling of processes, archiving, and compliance tracking—ensuring traceability, version control, and readiness for audits and submissions in a highly regulated environment. Additionally, you will be expected to: Sustain and improve document control systems across Neuralink in alignment with FDA regulations (e.g., 21 CFR Part 11, 21 CFR 58, 21 CFR 812) and other GxP requirements Organize GxP files (including study records, lab data, equipment logs, and audit documentation) into a traceable, trackable, and searchable system Maintain archives for GxP studies and ensure proper retention, deprecation, and re-indexing as needed (including leading archive re-indexing projects to correct/improve indexing) Assist in SOP development, revisions, periodic reviews, and maintenance of tables of contents Assist with the maintenance of various study trackers, training assignments, master schedule(s), and the glossary Facilitate the completion of deviations and investigations Manage document lifecycles: versioning, deprecation of obsolete documents, and routing/approval workflows Support the Regulatory department by organizing regulatory filings (e.g., new study submissions and supplements), managing uploads to the eTMF, and preparing routine submission documents (cover letters, annual reports) Required Qualifications: Meticulous attention to detail and exceptional organizational skills Excellent verbal and written communication skills Strong multitasking abilities in a dynamic, fast-paced, and constantly changing environment Proficiency with Google Suite (Docs, Sheets, etc.) and standard document management tools Working knowledge of medical, scientific, and regulatory terminology Preferred Qualifications: Bachelor's Degree in a relevant field, such as life sciences, engineering, technical writing/communications, regulatory affairs, or equivalent Relevant experience working in highly regulated environments, such as the medical device or pharmaceutical industries Expected Compensation: At Neuralink, your base pay is one part of your total compensation package. The anticipated hourly rate for this position is expected to be within the below range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. Texas Hourly Range: $21 – $35/Hr USD What We Offer: Full-time employees are eligible for the following benefits listed below. An opportunity to change the world and work with some of the smartest and most talented experts from different fields Growth potential; we rapidly advance team members who have an outsized impact Excellent medical, dental, and vision insurance through a PPO plan Paid holidays Commuter benefits Meals provided Equity (RSUs) *Temporary Employees & Interns excluded 401(k) plan *Interns initially excluded until they work 1,000 hours Parental leave *Temporary Employees & Interns excluded Flexible time off *Temporary Employees & Interns excluded

Responsibilities

This role supports company-wide document control activities, focusing on organizing and managing critical documentation across preclinical, manufacturing, engineering, quality, and regulatory departments. Responsibilities include sustaining and improving document control systems in alignment with FDA regulations and GxP requirements, managing document lifecycles, and supporting regulatory filings.