# Regulatory Engineer at Neuralink

Regulatory Engineer at Neuralink in Austin, Texas, United States. Full-time. Posted May 20, 2026.

- Company: Neuralink
- Location: Austin, Texas, United States
- Job type: Full-time
- Experience: 1+ year
- Posted: 2026-05-20
- Apply: https://boards.greenhouse.io/neuralink/jobs/7741688003?gh_jid=7741688003
- Source: https://jobmagic.ai/jobs/regulatory-engineer-neuralink-21hc5n

## Requirements

- Bachelor’s Degree or higher in an applicable engineering discipline (e.g., biomedical, mechanical, manufacturing, electrical, software, etc.)
- Strong technical writing and communication skills — ability to explain complex engineering concepts clearly and concisely.
- Excellent collaboration and organizational skills; comfort working in a fast-moving, cross-functional environment.

## 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 Regulatory Team, where our mission is to enable global access to Neuralink’s technology. We are a group of industry-experienced professionals who utilize creative problem-solving to establish efficient systems for maintaining the pace of innovation within highly regulated environments.

**Job Description and Responsibilities:**

As a Regulatory Engineer at Neuralink, you will be responsible for regulatory affairs activities and interactions with international regulatory bodies during clinical evaluations and/or market introduction, as well as compliance and reporting activities in the post-market phase. Additionally, you will develop regulatory approaches for devices under development, prepare pre-market regulatory submissions, and create post-approval reports. Furthermore, you will be expected to:

- Partner directly with R&D, hardware, software, and preclinical teams to integrate regulatory requirements into product architecture, testing strategies, and development roadmaps.

- Evaluate device classification, risk profiles, and global approval pathways, then design efficient technical solutions and documentation strategies that accelerate timelines.

- Identify regulatory and compliance obstacles early, anticipate emerging issues, and propose creative, data-driven workarounds, design refinements, or filing strategies that maintain innovation speed.

- Prepare high-quality regulatory submissions (IDE, PMA, international equivalents, supplements, dossiers, etc.) by organizing technical evidence, preclinical data, clinical results, and other materials into clear, compelling packages.

- Assess proposed design, manufacturing, preclinical, clinical, and testing changes for regulatory impact and develop appropriate filing strategies.

- Build and improve internal tools, templates, SOPs, and processes that make regulatory compliance faster and less burdensome for engineering teams; provide training to stakeholders to ensure organization-wide compliance.

- Stay technically current on evolving global standards, translate them into actionable guidance for designers, test engineers, and clinical teams, and distribute updated regulatory intelligence across the organization.

- Contribute to cross-functional problem-solving on topics ranging from biocompatibility and electromagnetic compatibility to software validation and human factors.

**Required Qualifications: 
**

- Bachelor’s Degree or higher in an applicable engineering discipline (e.g., biomedical, mechanical, manufacturing, electrical, software, etc.)

- Strong technical writing and communication skills — ability to explain complex engineering concepts clearly and concisely.

- Excellent collaboration and organizational skills; comfort working in a fast-moving, cross-functional environment.

**Preferred Qualifications: 
**

- 1+ years of experience in regulatory submissions, technical documentation, or quality engineering for medical devices (IDE, PMA, 510(k), international filings, etc.).

- Hands-on background in medical device design, testing, risk management (ISO 14971), or preclinical/clinical studies.

- Experience with class III/II medical device design, manufacturing, testing, and/or regulatory processes.

**Expected Compensation:**

The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:$71,000—$119,000 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*