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Biomedical Software Jobs in Austin, TX (NOW HIRING)

Quality Sr Engineer II

Austin, TX ยท 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 ...

... Software teams to create requirements from User Needs, perform Systems and Risk Analysis, and ... Masters or PhD degree in Engineering (Biomedical, Electrical, or Computer Science) * Minimum ...

Senior Lab Automation Engineer

Austin, TX ยท On-site

$106K - $133K/yr

Bachelor's degree in Biomedical Engineering, closely related scientific field or equivalent. * 4+ ... Software development experience, or minimally familiar with software development practices.

Sr. Quality Engineer

Austin, TX ยท On-site

$120 - $180/hr

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

Regulatory Engineer

Austin, TX ยท 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 ...

Sr. Quality Engineer

Austin, TX ยท On-site

$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 ...

Sr. Quality Engineer

Austin, TX ยท On-site

$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 ...

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 ...

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 ...

Showing results 41-60

Biomedical Software information

See Austin, TX salary details

$15

$28

$38

How much do biomedical software jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for biomedical software in Austin, TX is $28.27, according to ZipRecruiter salary data. Most workers in this role earn between $24.09 and $31.92 per hour, depending on experience, location, and employer.

What is the difference between Biomedical Software vs Biomedical Engineer?

AspectBiomedical SoftwareBiomedical Engineer
Required CredentialsTypically requires a degree in software engineering, computer science, or related fields; certifications in software development are commonRequires a degree in biomedical engineering, electrical engineering, or related fields; licensure or certification may be needed for clinical work
Work EnvironmentPrimarily in software development settings, labs, or healthcare IT departmentsHospitals, research labs, medical device companies, or manufacturing facilities
Employer & Industry UsageTech companies, healthcare IT firms, research institutionsMedical device manufacturers, hospitals, research organizations

Biomedical Software professionals focus on developing and maintaining software solutions used in healthcare, such as electronic health records or medical imaging software. Biomedical Engineers design and improve medical devices and equipment. While both roles work within the healthcare industry, Biomedical Software specialists concentrate on software development, whereas Biomedical Engineers work on hardware and device design.

What does a biomedical software engineer do?

A biomedical software engineer designs, develops, and tests software applications used in healthcare and medical research, such as imaging systems, electronic health records, and diagnostic tools. They often work with programming languages like C++, Java, or Python and collaborate with medical professionals to ensure software meets clinical needs and regulatory standards.

What cities near Austin, TX are hiring for Biomedical Software jobs?

Cities near Austin, TX with the most Biomedical Software job openings:

Infographic showing various Biomedical Software job openings in Austin, TX as of June 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $58,811 per year, or $28.3 per hour.

Quality Sr Engineer II

Zimmer, Inc.

Austin, TX โ€ข On-site

$87K - $118K/yr

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.


What You Can Expect

The Senior Quality Engineer II provides technical expertise in design assurance and system-level quality forClass II robotic medical devices. This role ensures compliance with FDA, ISO 13485, and ISO 14971 requirementsthroughout product development and design transfer. The Senior QE II partners with R&D, Systems, andElectrical/Mechanical Engineering teams to proactively manage product risk, verify design robustness, and ensurethe highest standards of safety, reliability, and performance. May mentor junior staff within the department.

Monogram's surgeon-guided semi- and fully autonomous robotic technologies are expected to add new anddifferentiated capabilities to Zimmer Biomet's already broad suite of customer-centric technology solutions. Byjoining this team you will be taking part in cutting edge technology used to improve patient outcomes and relievepain for patients across the globe. Excited to join us? Submit your application now.

This position is onsite, 5 days per week in Austin, Texas.

How You'll Create Impact
  • Support design assurance for assigned robotic system programs, ensuring design control deliverables comply with 21 CFR 820.30, ISO 13485, and internal procedures.
  • Support the development and maintenance of risk management files per ISO 14971, including system-level DFMEA, use-related risk analysis, and risk traceability to design mitigations.
  • Review and approve design verification and validation plans, protocols, and reports to confirm product performance and regulatory compliance.
  • Provide quality input during requirements definition, design reviews, and system integration phases to identify potential failure modes early.
  • Ensure robust traceability between design inputs, risk controls, verification, and validation activities.
  • Collaborate with Software Quality, Supplier Quality, and Manufacturing partners to ensure alignment across design and production readiness.
  • Participate in DFX (Design for Manufacturability, Reliability, Serviceability, and Testability) reviews and ensure that quality requirements are incorporated into design outputs.
  • Contribute to and continuously improve the Design Control and Risk Management procedures within the Quality Management System (QMS).
  • Support internal and external audits, CAPA investigations, and regulatory submissions with design assurance documentation.
  • Mentor and coach engineers in design assurance principles, quality engineering methods, and compliance practices.

This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.

What Makes You Stand Out
  • Comprehensive knowledge of FDA QSR (21 CFR 820), ISO 13485, and ISO 14971.
  • Strong expertise in design controls, risk management, and verification/validation activities for complex electromechanical or robotic systems.
  • Working knowledge of software and electronics integration sufficient to collaborate effectively with Software and Systems Quality teams.
  • Proficiency in FMEA, fault tree analysis, root cause investigation, and statistical analysis (SPC, capability, DOE).
  • Demonstrated ability to influence R&D and cross-functional teams in adopting quality-by-design principles.
  • Excellent written and verbal communication skills, with experience authoring and reviewing technical documentation for regulatory compliance.
  • Experience supporting design transfer and cross-functional development environments.
Your Background

Minimum Requirements: Bachelor's Degree in Engineering and 5 years of relevant experience or equivalent experience.

Preferred:

  • Bachelor's Degree in Mechanical, Electrical, Systems, Biomedical or Robotic Engineering.
  • 5+ years of experience in medical device engineering, inluding design assurance or development quality.
  • Experience with robotic or complex electromechanical systems.
  • Certiciation such as ASQ, CQE or CQA desirable.
Travel Expectations

Up to 20%


EOE

Employment Type: OTHER