Описание
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.
, 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 r
Контакты работодателя (email/phone/telegram) скрыты из публичного превью —
отправьте резюме, чтобы мы связали вас напрямую.