Medical Device Software Engineer (Associate) – Growth & Impact

Abbott Laboratories; Plymouth (MN); On-site; USD 51,000 - 101,000; Full time

Benefits offered by this job

Health insurance

Tuition reimbursement

Retirement savings plan

Education assistance

Job summary

Abbott is seeking a Software Engineer to design, develop, verify, and maintain software for structural heart devices at the Plymouth, MN site. You will work across the software lifecycle, including testing, system integration, and regulatory compliance in a quality-driven environment.

You will collaborate with Systems Engineering, Quality, Regulatory Affairs, Cybersecurity, and Product Development to deliver safe and effective solutions that improve patient outcomes.

Qualifications

• Bachelor's degree in a technical field and 0-2 years of related work experience.
• Strong programming skills in object-oriented software development.
• Understanding of software development lifecycle methodologies and testing practices.
• Experience with source control and version management tools.

Responsibilities

• Design, develop, test, and maintain software applications and system components.
• Participate in software verification and validation activities at unit, integration, and system levels.
• Develop, execute, and document software test procedures and results.
• Contribute to software quality initiatives including code reviews and defect resolution.
• Support automated test solutions and CI pipelines.
• Follow software development processes and document decisions throughout the product lifecycle.

Skills

C++

C#

Python

Git

CMake

Qt

Embedded Linux

CI/CD

Education

Bachelor's degree in Computer Science, Software Engineering, Computer Engineering, Electrical Engineering, or a related technical discipline

Tools

Git

CMake

Qt

Python

CI/CD tooling

Linux

Job description

Abbott is seeking a Software Engineer to design, develop, verify, and maintain software for structural heart devices at the Plymouth, MN site. You will work across the software lifecycle, including testing, system integration, and regulatory compliance in a quality-driven environment.

You will collaborate with Systems Engineering, Quality, Regulatory Affairs, Cybersecurity, and Product Development to deliver safe and effective solutions that improve patient outcomes.