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Microsoft Biomedical Engineering Jobs in Austin, TX

Bachelor's degree in biology, neuroscience, biomedical engineering, animal science, or a related ... Excellent attention to detail and proficiency in data compilation, documentation, and Microsoft ...

Sustaining Engineer I

Austin, TX · On-site

$75 - $95/hr

COMPANY OriGen Biomedical, Inc., is a global leader in cryopreservation and cell culture. We ... Bachelor's degree in Engineering OR 4+ years' experience in engineering principals of medical ...

Sustaining Engineer I

Austin, TX

$91K - $112K/yr

COMPANY OriGen Biomedical, Inc., is a global leader in cryopreservation and cell culture. We ... Bachelor's degree in Engineering OR 4+ years' experience in engineering principals of medical ...

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Microsoft Biomedical Engineering information

See Austin, TX salary details

$40.6K

$94K

$138.8K

How much do microsoft biomedical engineering jobs pay per year?

As of Aug 23, 2026, the average yearly pay for microsoft biomedical engineering in Austin, TX is $93,974.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,800.00 and $115,000.00 per year, depending on experience, location, and employer.

What is a Microsoft biomedical engineering?

A Microsoft Biomedical Engineering job involves applying engineering principles, software development, and AI to healthcare and life sciences. Professionals in this role work on innovative solutions such as medical imaging, wearable health technology, and AI-powered diagnostics. They collaborate with researchers, clinicians, and software engineers to develop tools that enhance patient care and medical research. This role combines expertise in biomedical engineering, machine learning, and cloud computing to create cutting-edge healthcare technologies.

What does a Microsoft biomedical engineering do?

As a Microsoft Biomedical Engineering professional, your day-to-day tasks may include developing and testing software solutions for healthcare applications, collaborating with clinicians and researchers to understand user needs, and integrating medical data using Microsoft cloud technologies. You may also troubleshoot system issues, ensure data security compliance, and participate in multidisciplinary meetings to drive project progress. The role typically involves working closely with other engineers, data scientists, and healthcare providers, providing a dynamic and collaborative work environment where innovation and technical expertise are highly valued.

What are the key skills and qualifications needed to thrive in the Microsoft biomedical engineering position, and why are they important?

To thrive as a Microsoft Biomedical Engineering professional, a strong background in biomedical engineering, computer science, and data analysis is essential, typically supported by a relevant engineering degree. Familiarity with Microsoft cloud platforms (such as Azure), programming languages like Python or C#, and experience with healthcare standards (like HL7 or DICOM) are highly valued. Excellent problem-solving, communication, and teamwork skills help professionals excel in cross-functional environments. These skills enable effective development and deployment of innovative healthcare technology solutions that improve patient outcomes.

What are the most commonly searched types of Microsoft Biomedical Engineering jobs in Austin, TX?

The most popular types of Microsoft Biomedical Engineering jobs in Austin, TX are:

What are popular job titles related to Microsoft Biomedical Engineering jobs in Austin, TX?

For Microsoft Biomedical Engineering jobs in Austin, TX, the most frequently searched job titles are:

Infographic showing various Microsoft Biomedical Engineering job openings in Austin, TX as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $93,974 per year, or $45.2 per hour.

Preclinical Study Coordinator

Neuralink

Austin, TX • On-site

Full-time

Re-posted 23 days ago


Job description

Team Description:

The Preclinical Team is responsible for designing, conducting, documenting, analyzing, and reporting preclinical studies. Our team provides a means for ensuring the safe, effective, and robust implantation of Neuralink devices into animals and, ultimately, humans.

Job Description and Responsibilities:

The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of day-to-day coordination, scheduling, data compilation, and administrative tasks, enabling the Study Director to focus on scientific oversight, data interpretation, and regulatory compliance. The Study Coordinator acts as a key liaison across the preclinical team, technical staff, and cross-functional groups to ensure studies progress smoothly, on time, and in compliance with protocols and SOPs. The Study Coordinator will:

  • Support the Study Director in developing study protocols, amendments, and related documentation.
  • Facilitate cross-functional communication, establish and track study timelines, and prepare/lead study milestone meetings.
  • Identify and help eliminate roadblocks that could delay study progress.
  • Assist with implementation of test methods and practices described in the study protocol and SOPs.
  • Help ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified.
  • Manage the study schedule, alerting the Study Director and team to critical data collection points or deadlines.
  • Support the documentation and addressing of self-reported or QAU-generated deviations that may affect study quality.
  • Compile data, organize contributing scientist reports, and assist in preparing the final study report so it accurately reflects study results.
  • Maintain organized study files, track communications, and support archiving of data, documentation, protocols, specimens, and reports per GLP.
  • Coordinate day-to-day study activities with technical staff, veterinary teams, and external partners (e.g., CROs if applicable).
  • Contribute to internal tracking systems, meeting minutes, and status updates for the Preclinical Team.

Required Qualifications:

  • Bachelor's degree  in biology, neuroscience, biomedical engineering, animal science, or a related field.
  • Minimum 1 year of experience in preclinical research support, study coordination, or project management (academic experience applies).
  • Solid understanding of GLP regulations (21 CFR Part 58), basic knowledge of ISO 10993, and familiarity with in vivo animal studies.
  • Strong organizational and project management skills with proven ability to manage timelines and multiple priorities.
  • Excellent attention to detail and proficiency in data compilation, documentation, and Microsoft Office (or equivalent) tools.
  • Experience working in or supporting animal research facilities with IACUC protocols.

Preferred Qualifications:

  • Master's degree  in biology, neuroscience, biomedical engineering, animal science, or a related field.
  • Direct experience with neural device implantation studies or neurosurgical models.
  • Background in a CRO or medical device preclinical setting.
  • Familiarity with electronic data capture systems or GLP-compliant documentation platforms.

Additional Requirements and Competencies:

  • Willingness to work in an animal research facility environment (with required training and PPE).
  • Flexibility in schedule to support critical study timepoints.