Document Control Specialist

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 and other GxP requirements, organize GxP files, maintain archives for GxP studies, assist in SOP development and revisions, facilitate the completion of deviations and investigations, manage document lifecycles, and support the Regulatory department.