Document Control Specialist • Mid-Level

Who you are

You have strong organizational skills and a keen eye for detail, which are essential for managing critical documentation across various departments including preclinical, manufacturing, engineering, quality, and regulatory. Your experience in document control systems ensures that you can maintain compliance and readiness for audits in a highly regulated environment.

You understand the importance of traceability and version control, especially in the context of FDA regulations such as 21 CFR Part 11, 21 CFR 58, and 21 CFR 812. Your ability to organize GxP files into a traceable, trackable, and searchable system is crucial for the success of the Quality Team at Neuralink.

What you'll do

In this role, you will support the maintenance, development, and scaling of document control processes across the organization. You will be responsible for organizing GxP files, including study records, lab data, equipment logs, and audit documentation, ensuring they are easily accessible and compliant with regulatory standards. You will also work closely with various teams to sustain and improve document control systems, contributing to the overall quality and compliance framework at Neuralink.

What we offer

Neuralink provides excellent medical, dental, and vision insurance through a PPO plan, along with paid holidays and commuter benefits. Meals are provided, and employees have the opportunity to participate in an equity program (RSUs). We also offer a 401(k) plan and flexible time off, ensuring a supportive work environment for all team members.