Software Quality Engineer II - Firmware & QA (Onsite CA)

Abbott; Los Angeles (CA); On-site; USD 82,000 - 141,000; Full time

Benefits offered by this job

Free HIP PPO medical plan

Excellent retirement plan

Tuition reimbursement

FreeU education benefit

Great place to work

Job summary

Abbott Laboratories in Sylmar, CA is seeking a Software Development Quality Engineer to support the design and development of firmware and communication software, as well as non-product software and automated manufacturing tests.

The role emphasizes quality processes, DHF/Documentation, and adherence to FDA/regulatory requirements while collaborating with cross-functional teams to protect patient safety and meet business needs.

Qualifications

• Bachelor's degree in Engineering or technical field.
• Minimum 2 years in software development and/or embedded systems.
• 2–5+ years in software testing and verification/validation.
• Programming in C/C++, C#, Python, Java.
• Experience with Git, Jira, Subversion, DOORS, Bugzilla, or equivalent.
• Experience with static analysis tools and test-driven development.

Responsibilities

• Plan, execute, and complete quality engineering deliverables including test plans, procedures, scripts, and reports.
• Lead and coordinate test planning and execution across cross-functional teams.
• Apply testing methodologies, tools, templates, and environments to support projects.
• Communicate testing strategies and quality concepts to team members and partners.
• Develop and maintain SOPs, specifications, and test procedures per QMS.

Skills

C/C++

Python

Embedded systems

Software testing

Agile/Scrum

Java

Education

Bachelor's degree in Engineering

Tools

Git

Jira

DOORS

Bugzilla

Static analysis tools

Code review tools

Job description

Abbott Laboratories in Sylmar, CA is seeking a Software Development Quality Engineer to support the design and development of firmware and communication software, as well as non-product software and automated manufacturing tests.

The role emphasizes quality processes, DHF/Documentation, and adherence to FDA/regulatory requirements while collaborating with cross-functional teams to protect patient safety and meet business needs.