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Software Quality Engineer Intern Jobs in Austin, TX

As a Software Engineer Intern on the Brain Interfaces Software Team, your responsibilities will encompass: * Developing and improving Neuralink's Implant and Charger SDK * Maintaining Neuralink ...

As a Software Engineer Intern on the Brain Interfaces Software Team, your responsibilities will encompass: * Developing and improving Neuralink's Implant and Charger SDK * Maintaining Neuralink ...

About the Role As a Software QA Engineer, you will work closely with engineers and product teams to make sure our software works as intended and remains reliable as it changes. You will help ...

Software Quality Sr Engineer

Austin, TX · On-site

$100K - $124K/yr

What You Can Expect The Monogram Technologies Team at Zimmer Biomet is seeking a detail-oriented Software Validation and Quality Sr Engineer experienced in regulated environments, specializing in ...

... 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 ...

Construction Scheduling Intern As a Construction Scheduling Intern at Ryan, you'll work side by ... Along the way you'll build real skills in CPM scheduling, scheduling software, contracts and the ...

Showing results 21-40

Software Quality Engineer Intern information

See Austin, TX salary details

$13

$25

$38

How much do software quality engineer intern jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for software quality engineer intern in Austin, TX is $25.19, according to ZipRecruiter salary data. Most workers in this role earn between $20.48 and $28.61 per hour, depending on experience, location, and employer.

What does a software quality engineer intern do?

A Software Quality Engineer Intern assists in ensuring the quality and reliability of software products by executing tests, identifying bugs, and reporting issues to the development team. They may help design test cases, automate testing processes, and document results. Interns often work closely with senior quality engineers and developers to learn best practices and contribute to the overall improvement of software quality. Their role provides valuable hands-on experience in software development and quality assurance processes.

What are the key skills and qualifications needed to thrive as a software quality engineer intern?

To thrive as a Software Quality Engineer Intern, you need a solid understanding of software development fundamentals, testing methodologies, and a relevant academic background in computer science or a related field. Familiarity with automated testing tools like Selenium, version control systems such as Git, and bug tracking platforms like Jira is typically expected. Attention to detail, analytical thinking, and effective communication are crucial soft skills for this role. These skills and qualities are important to ensure software reliability, support collaboration with development teams, and contribute to the delivery of high-quality products.

What are some typical challenges a software quality engineer intern might face during their internship?

As a Software Quality Engineer Intern, you may encounter challenges such as quickly learning new testing tools and methodologies, understanding complex codebases, and adapting to agile development cycles. Balancing multiple tasks, such as writing test cases, executing manual tests, and collaborating with developers to troubleshoot bugs, can also be demanding. However, these experiences offer valuable opportunities to develop technical skills, improve communication, and gain insight into the software development lifecycle in a team-oriented environment.

What is the difference between Software Quality Engineer Intern vs Software Tester Intern?

AspectSoftware Quality Engineer InternSoftware Tester Intern
Required CredentialsTypically pursuing or recent graduate in Computer Science or related fieldSimilar educational background, often pursuing or recent graduate in related fields
Work EnvironmentInvolves collaboration with development teams, understanding testing processes, and quality assuranceFocuses on executing test cases, reporting bugs, and verifying fixes
Employer & Industry UsageUsed across software companies, tech firms, and QA departmentsCommonly used in software development and testing teams

The main difference is that a Software Quality Engineer Intern has a broader role involving quality processes, test planning, and collaboration, while a Software Tester Intern primarily focuses on executing tests and identifying bugs. Both roles require similar educational backgrounds and are used in similar environments, but the Quality Engineer Intern has a more comprehensive scope in quality assurance activities.

What are the most commonly searched types of Software Quality Engineer jobs in Austin, TX?

The most popular types of Software Quality Engineer jobs in Austin, TX are:

What cities near Austin, TX are hiring for Software Quality Engineer Intern jobs?

Cities near Austin, TX with the most Software Quality Engineer Intern job openings:

Quality Engineer, Software Design Controls

Austin, TX • On-site

Neuralink
Biotechnology Research and Development • 201 - 500 employees

Full-time

Medical, Dental, Vision, Retirement

Posted 19 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