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Urgent! Staff Software Engineer Job Opening In Irving – Now Hiring Abbott

Staff Software Engineer



Job description

The Opportunity

This position works out of our Irving, TX or Santa Clara, CA locations in the Core Diagnostics Business Group.

Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe.

The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

We are seeking an experienced and independent Staff Software Engineerto join our Hematology Division, supporting the development and maintenance of advanced blood testing instruments.

This role is critical to both new product development and the resolution of escalated technical issues.

You will work in a dynamic, high-volume environment alongside a small, collaborative team split into Front-End and Data Processing sub-teams.

What You’ll Work On

  • Supports hematology instruments used in blood testing and analysis.

  • Two sub-teams:Front-End Engineering (FSE)andData Processing.

  • High interdependency and collaboration; flexibility and coordination are essential.

  • Fast-paced, rapidly evolving environment with high expectations for quality and responsiveness.

  • Ideal forseasoned, independent engineerswho thrive in dynamic settings

  • Participate innew developmentof software for hematology instruments.

  • Investigate and resolveescalated product complaints.

  • Design and implementsoftware changes and enhancements.

  • Conducttesting on actual instrumentsto validate functionality.

  • Performformal code reviewsand ensure adherence to quality standards.

  • Write and executedevelopment-level testsfor new and modified code.

  • Executehigh-paced validation and verificationactivities.

  • Addressnon-conformancesand supportfinal releaseprocesses.

  • Collaborate with management onquality and complianceaspects.

  • Focus onC++ coding, debugging, and validation in a regulated environment.

  • May conduct design analysis on components and/or assemblies to assist in the development process by ensuring designs are cost efficient, manufacturable, and reliable.

  • Communicates with the other engineering personnel to coordinate the interrelated design and assure project completion.

  • May act as internal consultant providing technical guidance on most complex projects.

  • This is a non-supervisory position.

  • Follows defined software development lifecycle procedures and

  • Abbott's quality system procedures.

  • Expert in local software development procedures.

  • Supports mentoring junior level engineers on Abbott and local processes and practices 

  • May participate in CFT team to identify and implement improvements to local procedures.

  • Required Qualifications:

  • Bachelor’s degreein Computer Science, Software Engineering, Biomedical Engineering, or a related field.

  • 8+ years of related experience or a Master’s degree and 6+ years of related experience preferably in medical devices or regulated industries.

  • Proficiency inC++and experience with embedded systems or instrument control.

  • Strong understanding ofsoftware validation,code reviews, andquality assurancepractices.

  • Preferred Qualifications:

  • Experience in themedical device industryor other regulated environments (e.g., FDA, ISO 13485).

  • Excellent problem-solving skills and ability to work independently in a fast-changing environment.

  • Familiarity withinstrumentation,data processing, orfront-end engineering.

  • Knowledge ofsoftware lifecycle processesandrisk management.

  • Able to work variable hours.

  • Ability to work on site.


  • Required Skill Profession

    Computer Occupations



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      Unlock Your Staff Software Potential: Insight & Career Growth Guide


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