Staff Software Engineer

Abbott (abbottcareers2 board); United States; Presencial; USD 140 000 - 210 000; Tempo integral

Resumo da oferta

Abbott is seeking a Staff Software Engineer in Plano, TX to lead software automation, integration, and quality across the full development life cycle for safety-critical, connected medical devices. The role emphasizes hands-on leadership, AI-enabled engineering, and adherence to medical device standards.

You will set the technical direction, mentor teams, and partner with software, systems, quality, cybersecurity, and product teams to raise the bar on quality and delivery.

Qualificações

• Bachelor degree in a relevant field.
• Experience leading automation and quality efforts for safety-critical software.
• Experience with medical devices or regulated environments is a plus.

Responsabilidades

• Set the automation and quality strategy across product lines.
• Architect reusable automation frameworks, services, and tools.
• Embed automated quality controls into CI/CD pipelines.
• Engineer connected-system integration across devices and applications.
• Apply responsible AI principles in engineering workflows.
• Lead technical quality and mentor teams while remaining hands-on.
• Ensure safety and compliance with IEC 62304, ISO 14971, ISO 13485, and 21 CFR 820.

Conhecimentos

Automation strategy

Quality engineering

CI/CD

AI integration

Software architecture

Embedded software

Leadership

Safety-critical software

Formação académica

Bachelor

Ferramentas

CI/CD pipelines

Embedded device interfaces

Descrição da oferta de emprego

JOB DESCRIPTION:

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Job Title

Staff Software Engineer

Working at Abbott

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Plano, Texas location in the Neuromodulation Division. Our Neuromodulation business includes implantable devices compatible with mobile technology to help people who suffer from chronic pain and movement disorders. These non-opioid therapies allow us to provide interventional pain therapy to patients throughout the pain continuum.

For more than 135 years, Abbott has helped people around the world live fuller, healthier lives through the right combination of science and technology. We are looking for a Staff-level technical leader to architect and advance software automation, integration, and quality engineering across the full software development life cycle for safety-critical, connected medical devices.

This is a hands-on software engineering leadership role centered on scalable test automation and continuous verification-not a traditional, script-heavy QA position. You will embed quality from requirements and design through implementation, integration, release, and maintenance. You will also apply AI tools responsibly in daily engineering work, using human oversight, traceability, privacy, security, and measurable evidence to improve-not replace-engineering judgment. As a Staff Engineer, you will set technical direction, raise the engineering bar across teams, and mentor others while remaining deeply hands-on.

What you’ll work on

• Set the automation and quality strategy. Define the vision, reference architecture, and roadmap for scalable automation and continuous verification across product lines, and drive adoption as a recognized technical authority.
• Architect lifecycle automation. Design and build reusable frameworks, services, simulators, and engineering tools that enable requirements-based and risk-based verification at the unit, component, integration, system, regression, and release levels.
• Integrate quality into delivery. Embed automated quality controls, traceability, diagnostics, and actionable quality signals into CI/CD pipelines so teams receive rapid, reliable feedback throughout the development life cycle.
• Engineer connected-system integration. Develop robust integration capabilities across embedded devices, clinician applications, interfaces, services, data flows, and representative hardware or simulated environments.
• Apply AI responsibly. Incorporate Abbott's Responsible, Safe, Transparent, Fair, and Impactful AI principles into daily automation and quality engineering. Follow established governance and intended-use boundaries; protect sensitive data; verify generated outputs; preserve source traceability; document limitations; and maintain meaningful human oversight and accountability.
• Advance AI-enabled engineering. Use AI copilots, large language models, and agentic workflows to improve coverage analysis, automation development and maintenance, failure investigation, and engineering productivity where their use is appropriate, validated, reproducible, and auditable.
• Lead technical quality. Partner with software, systems, quality, cybersecurity, and product teams to improve architecture, prevent defects, close coverage gaps, strengthen design reviews, and make quality measurable across programs.
• Ensure safety, compliance, and continuous improvement. Keep automation and AI-assisted engineering aligned with applicable medical device standards, including IEC 62304, ISO 14971, ISO 13485, and 21 CFR 820. Evaluate emerging tools, measure their impact on product quality and delivery, scale proven approaches, and mentor engineers in their effective and responsible use.

Required Qualifications

Bachelor