Software Quality, Engineer II
AbbottAbout the role
JOB DESCRIPTION:
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
Career development with an international company where you can grow the career you dream of .
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with 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 around the world and named one of the most admired companies in the world by Fortune.
The Opportunity
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division.
As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.
We are seeking a high caliber Software Quality Engineer II supporting the DevOps functions. Working under general supervision, provides quality oversight to development and production operation activities including, but not limited to, planning, and coordinating software deployment, implementation of various services involving on-prem and Cloud, developing and maintaining software tools, supporting and troubleshooting applications. You will be working on various Cloud services and also provide quality oversight to our existing operations hosted on-prem which includes managing several java applications, support middleware technologies, continuous automation, adapt Site reliability engineering (SRE) principles to operations problems and drive quality, compliance, security initiatives.
What You’ll Work On
Has good understanding of the software programming, agile software development, database management, networking concepts, cybersecurity, and cloud computing.
Supports deployment of CI/CD pipelines and demonstrate scripting skills through Ruby, Python, Shell or other scripting languages.
Supports release and deployment of code from Development, Test, Stage and Production environments
Applies risk management principles to all activities and tasks to investigate non-conformances. Identifies areas for process improvement and provides supporting information for change, including reasons and justifications.
Participates in the development or modification of verification/validation packages and deliverables, including, assessments (including risk assessments, e.g., FMEAs), plans, requirements, and protocols.
Ensure compliance to relevant FDA QSR, ISO guidelines, including 21 CFR Part 11 and Abbott Corporate requirements as they relate to the development, validation and maintenance of computerized systems.
Create and execute or direct software validation protocols traceable to system/software requirements. Execute and support on-time completion of Quality Engineering deliverables: test plans (manual and automated), test scripts (manual and automated), test reports
Implement solutions for controlling code and administer Code Control and Software Event/Defect Tracking software systems.
Design and implement various product and process improvement methodologies (i.e, Six Sigma and Lean Manufacturing).
Apply sound, systematic problem solving methodologies in identifying, prioritizing, communicating and resolving issues.
Support internal (corporate and divisional) and external quality audit
Support all Company initiatives as identified by management and in support of Quali
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