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Content Risk Reviewer Jobs in Austin, TX (NOW HIRING)

Nintendo

Producer - Background Art (Retro Studios)

Austin, TX · On-site

$122K - $124K/yr

Coordinate and run sprint and milestone planning, reviews and retrospectives. * Track team velocity ... Share and refine risk mitigation strategies with Department Directors, Lead Producer and VP of ...

YO AI Labs

Hematology Expert - Remote

Austin, TX · Remote

$150 - $200/hr

In this role, you will help improve next-generation AI systems by evaluating clinical content ... Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ...

YO AI Labs

Oncology Expert - Remote

Austin, TX · Remote

$150 - $200/hr

In this role, you will help improve next-generation AI systems by evaluating clinical content ... Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ...

YO AI Labs

Clinicia Expert - Remote

Austin, TX · Remote

$150 - $200/hr

In this role, you will help improve next-generation AI systems by evaluating clinical content ... Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ...

Seon

Instructional Designer

Austin, TX · On-site

$85 - $125/hr

Select appropriate instructional strategies based on audience, content, and business goals in order ... review, and deployment. What you'll bring: * Demonstrated experience applying the ADDIE model (or ...

Nexzerz

PM_Project Manager 3

Austin, TX · On-site

Manage deliverable content expectations, review processes, and acceptance criteria. Ensure ... estimation, risk mitigation, and preventive and corrective actions for overruns. 8 Required ...

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Showing results 41-60

All JobsContent Risk Reviewer JobsContent Risk Reviewer Jobs in Austin, TX

Content Risk Reviewer information

What is the difference between Content Risk Reviewer vs Content Moderator?

AspectContent Risk ReviewerContent Moderator
CredentialsTypically requires familiarity with content policies, risk assessment, and sometimes certifications in compliance or content reviewOften requires knowledge of platform policies, communication skills, and sometimes basic certifications in social media or content management
Work EnvironmentUsually in office or remote settings, analyzing flagged content for potential risks or violationsPrimarily in social media, forums, or online platforms, monitoring live or flagged content
Employer & IndustryTech companies, social media platforms, online marketplacesSocial media companies, online forums, content sharing platforms

While both roles involve reviewing online content, Content Risk Reviewers focus on assessing potential risks and compliance issues, whereas Content Moderators primarily enforce platform policies by removing or flagging inappropriate content. The roles often overlap but differ in scope and focus.

How do I become a content risk reviewer?

To become a content risk reviewer, candidates typically need strong critical thinking skills, knowledge of platform policies, and experience with content moderation tools. Relevant qualifications often include a high school diploma or equivalent, and some roles may require familiarity with content management systems or basic understanding of online safety. Training is usually provided by the employer to ensure adherence to specific guidelines and standards.

What are popular job titles related to Content Risk Reviewer jobs in Austin, TX?

For Content Risk Reviewer jobs in Austin, TX, the most frequently searched job titles are:

What job categories do people searching Content Risk Reviewer jobs in Austin, TX look for?

The top searched job categories for Content Risk Reviewer jobs in Austin, TX are:

What cities near Austin, TX are hiring for Content Risk Reviewer jobs?

Cities near Austin, TX with the most Content Risk Reviewer job openings:

Content Risk Reviewer jobs near you
Infographic showing various Content Risk Reviewer job openings in Austin, TX as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution.

Quality Engineer, Software Design Controls

Neuralink

Austin, TX • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 17 days ago

Job 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 Translational Team, where we generate the data that advances Neuralink's brain-computer interface technologies from research and development through clinical evaluation and into market implementation. We produce the rigorous evidence required to support rapid development, regulatory progress, and the safe, effective delivery of the technology to patients.
Job Description and Responsibilities:
The Quality Engineer, Software Design Controls will own software design control strategy, processes, documentation, and continuous improvement across implantable electronics software, surgical robotics software, external systems, and related non-product software. Responsibilities include:
  • Work directly with software and firmware teams to identify design control and software lifecycle risks early, drive robust mitigations, and support design reviews to embed strong design control and IEC 62304 practices.
  • Own software design control impact assessments for design changes within the medical device design control process; evaluate effects on requirements, architecture, risk controls, verification/validation, and traceability; determine re-test, analysis, or documentation needs; and update risk assessments, protocols, and Design History File (DHF) content to maintain ongoing compliance.
  • Own end-to-end software design control strategy and plan/execute activities supporting the full software lifecycle (requirements, architecture, detailed design, implementation, verification, validation, risk management, and release) for Class III and other regulated software in accordance with IEC 62304, ISO 14971, ISO 13485, and related standards.
  • Debug software quality and design control gaps using requirements management tools, traceability matrices, code/architecture reviews, test results, anomaly data, and root-cause analysis techniques; recommend effective process and design mitigations.
  • Develop, execute, and maintain software design control deliverables including design and development plans, software requirements specifications, architecture documents, verification/validation plans and reports, risk management files, traceability matrices, change control records, and requirement-to-test linkages for complex systems involving implants, chargers, robots, and supporting software.
  • Stay current with advancements in medical device software standards, regulatory science, and related technologies; contribute to continuous improvement of compliance processes, SOPs, templates, and knowledge sharing across teams.

Required Qualifications:
  • Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or related technical discipline.
  • 3+ years of hands-on experience with software design controls, software quality, or software design assurance for medical devices.
  • Strong understanding of the software development lifecycle (SDLC) in regulated or safety-critical environments and practical application of design controls.
  • Direct experience planning, executing, reviewing, and documenting software design control and verification/validation activities.
  • Working knowledge of IEC 62304 (Medical Device Software Lifecycle Processes), ISO 14971 (Risk Management), and ISO 13485.
  • Strong cross-functional communication skills and ability to drive issues to closure across engineering, quality, regulatory, and external partners.

Preferred Qualifications:
  • Experience with implants, surgical robotics, wireless systems, or Software as a Medical Device (SaMD) / Software in a Medical Device (SiMD).
  • Prior experience contributing software design control or V&V data to regulatory submissions (IDE, 510(k), PMA, or equivalent) and interfacing with FDA or notified bodies.
  • Experience with medical device design controls, ISO 14971 risk management (including software FMEA / SFMEA), cybersecurity risk assessment, and product development lifecycle in a regulated environment.
  • Experience developing software design control guidelines, training programs, templates, or compliance workflows that accelerate product development.
  • Familiarity with additional standards such as IEC 62366 (usability), 21 CFR Part 11, or cybersecurity guidance (FDA, IEC 81001-5-1).
  • Experience writing test protocols, reports, deviations, engineering rationales, risk assessments, and requirement traceability in a regulated or quality-controlled development process.

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:
$103,000-$191,000 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

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