ZipRecruiter

Log In

1

Biomedical Software Engineer Jobs in Austin, TX (NOW HIRING)

Neuralink

Regulatory Engineer

Austin, TX · On-site

$71K - $119K/yr

Bachelor's Degree or higher in an applicable engineering discipline (e.g., biomedical, mechanical, manufacturing, electrical, software, etc.) * Strong technical writing and communication skills ...

Enovis

Principal Quality Engineer

Austin, TX · On-site

Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Manufacturing Engineering, or ... Review and approve software requirements, design documentation, risk management files, and test ...

Enovis

Sr. Quality Engineer

Austin, TX

$87K - $118K/yr

Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Manufacturing Engineering, or ... Review and approve software requirements, design documentation, risk management files, and test ...

Zimmer, Inc.

Quality Sr Engineer II

Austin, TX · On-site

$87K - $118K/yr

Collaborate with Software Quality, Supplier Quality, and Manufacturing partners to ensure alignment ... Preferred: * Bachelor's Degree in Mechanical, Electrical, Systems, Biomedical or Robotic ...

Zimmer, Inc.

Senior Systems Engineer

Austin, TX · On-site

$103K - $141K/yr

... Software teams to create requirements from User Needs, perform Systems and Risk Analysis, and ... Preferred: * BS degree in Engineering (Biomedical, Electrical, or Computer Science) * Work ...

OriGen Biomedical

Office Coordinator

Austin, TX · On-site

$27 - $33/hr

COMPANY OriGen Biomedical, Inc., is a global leader in cryopreservation and cell culture. We ... computer software and hardware applications, including Microsoft Word, Excel, and G-Suite. ● ...

Enovis

Design Quality Engineer

Austin, TX

Bachelor's in Biomedical or Mechanical Engineering and 3+ years of experience. * Background in ... Preferred knowledge of the following software packages: Solidworks, Solidworks ePDM, Oracle R12 ...

Enovis

Design Quality Engineer

Austin, TX · On-site

Bachelor's in Biomedical or Mechanical Engineering and 3+ years of experience. * Background in ... Preferred knowledge of the following software packages: Solidworks, Solidworks ePDM, Oracle R12 ...

CryoLife

Automated Inspection Quality Engineer

Austin, TX · On-site

$71K - $92K/yr

... biomedical, medical device field) with an in-depth knowledge of current Good Manufacturing ... software used in the receipt, testing, processing, storing, and distribution of raw materials ...

Artivion

Automated Inspection Quality Engineer

Austin, TX · On-site

$72K - $93K/yr

... biomedical, medical device field) with an in-depth knowledge of current Good Manufacturing ... software used in the receipt, testing, processing, storing, and distribution of raw materials ...

Pwc

Supply Chain Execution Manager

Austin, TX · On-site

$99K - $232K/yr

... Engineering & Management, Biomedical Science, Computer and Information Science, Data Processing/Analytics/Science - Demonstrating proficiency in Supply Chain Management Software - Utilizing strategic ...

DiaSorin

Field Service Engineer

Austin, TX

$69K - $117K/yr

Resolve instrument problems by troubleshooting the specific problem (hardware or software) and ... Minimum 2 Years as a Biomedical Equipment, Electronics or Field Service Technician, or equivalent ...

DiaSorin

Field Service Engineer

Austin, TX · On-site

$33.31 - $56.63/hr

Resolve instrument problems by troubleshooting the specific problem (hardware or software) and ... Minimum 2 Years as a Biomedical Equipment, Electronics or Field Service Technician, or equivalent ...

Pwc

Kinaxis Solutions Architect, Manager

Austin, TX · On-site

$99K - $232K/yr

... Engineering & Management, Biomedical Science, Computer and Information Science, Data Processing/Analytics/Science - Demonstrating proficiency in Supply Chain Management Software - Excelling in ...

previous pagenext page

Showing results 21-40

All JobsBiomedical Software Engineer JobsBiomedical Software Engineer Jobs in Austin, TX

Biomedical Software Engineer information

See Austin, TX salary details

$62.9K

$146.2K

$203.6K

How much do biomedical software engineer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for biomedical software engineer in Austin, TX is $146,192.00, according to ZipRecruiter salary data. Most workers in this role earn between $118,900.00 and $171,400.00 per year, depending on experience, location, and employer.

What does a biomedical software engineer do?

Biomedical Software Engineers often work on designing, developing, and maintaining software used in medical devices, clinical diagnostics, or healthcare information systems. Typical responsibilities include coding new features, troubleshooting and resolving software issues, ensuring compliance with medical standards, and participating in quality assurance testing. You may also collaborate closely with clinicians, researchers, and regulatory specialists to align technological solutions with user needs and safety requirements. These projects frequently involve iterative development and rigorous validation to ensure reliability in real-world medical settings.

What is a biomedical software engineer?

A Biomedical Software Engineer develops software solutions for medical and healthcare applications, including medical devices, diagnostic tools, and research simulations. They combine biomedical knowledge with software development skills to create and maintain systems that improve patient care, enhance medical research, and ensure regulatory compliance. Their work often involves programming, data analysis, and collaboration with healthcare professionals and researchers.

What skills and qualifications are needed to be a biomedical software engineer?

To thrive as a Biomedical Software Engineer, you need a strong background in computer science, biomedical engineering, and software development—often supported by a bachelor's or master's degree in a related field. Proficiency with programming languages such as Python, C++, or Java, familiarity with medical imaging tools, and experience working with healthcare interoperability standards like HL7 or DICOM are typically required. Effective communication, teamwork, and problem-solving skills are crucial for collaborating with cross-functional teams and understanding user requirements. These competencies ensure that biomedical software solutions are safe, compliant, and meet the complex needs of healthcare environments.

What are popular job titles related to Biomedical Software Engineer jobs in Austin, TX? For Biomedical Software Engineer jobs in Austin, TX, the most frequently searched job titles are:
What job categories do people searching Biomedical Software Engineer jobs in Austin, TX look for? The top searched job categories for Biomedical Software Engineer jobs in Austin, TX are:
What cities near Austin, TX are hiring for Biomedical Software Engineer jobs? Cities near Austin, TX with the most Biomedical Software Engineer job openings:
Biomedical Software Engineer jobs near you
Infographic showing various Biomedical Software Engineer job openings in Austin, TX as of August 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $146,192 per year, or $70.3 per hour.

Regulatory Engineer

Neuralink

Austin, TX • On-site

$71K - $119K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-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 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

Apply