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 114,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

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.
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 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.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

Our location in Sylmar, CA, currently has an onsite opportunity for a R&D Senior Software Engineer. 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.

What You’ll Work On

Supports the implementation, development, enhancement, and modification of software tools and applications to facilitate product development and verification.
Develops, maintains, and updates test requirements and designs based on requirement specifications.
Support verification activities within the group.
Identifies, debugs, and resolves software issues, providing strategic recommendations for future improvements.
Creates design concepts, including parameters, structure, and core components.
Participates in design reviews, documents findings, and addresses issues as directed.
Contributes to peer reviews on related projects, offering constructive feedback.
Assists in various development and testing phases as needed.
May draft and update requirement specifications for assigned areas.
Reviews project deliverables—such as specifications, code, and test/tool procedures—for feasibility, completeness, clarity, accuracy, and correctness.
Ensures compliance with U.S. Food and Drug Administration (FDA) regulations, other regulatory standards, company policies, operating procedures, and assigned tasks. Maintains positive and collaborative communication with employees, customers, contractors, and vendors at all levels.
Owns specific tasks within larger initiatives—such as user needs analysis, feature definition, validation, or subsystem development—and drives them to timely, high-quality completion.
Collaborates with internal teams, including Quality, as required.
Performs other related duties and responsibilities as assigned.

EDUCATION AND EXPERIENCE YOU’LL BRING

Required

Over 6 years of experience in software development, including programming-intensive coursework, academic projects, and professional roles.
Skilled in clearly communicating technical solutions and issues to both management and project team members.
Familiarity with software development processes for the medical device industry is a plus.
Test automation experience is a plus.
Experience with AI tools such as GitHub Copilot is a plus.Experience leading cross-site teams to work collaboratively is a plus.
Ability to identify and drive process improvement initiatives is a plus.
Proficient in capturing and analyzing customer requirements and translating them into effective design and solutions.
Preferred experience with programming languages such as C#, VB.NET, VC++, Java, ASP.NET or Python
Preferred experience with operating systems including Windows and Linux.
Knowledge of multitasking systems / real-time application development preferred.
Familiarity with Object-Oriented Analysis and Design (OOAD) concepts preferred.
Experience with tools such as Install Aware, AccuRev, Jira, Bit Bucket, Glib Repository, Microsoft Visual Studio and ClearQuest is a plus.
Strong analytical and problem-solving skills.
Ability to work effectively both independently and as part of a team in a fast-paced, dynamic environment.
Excellent verbal and written communication skills.

Preferred Qualification and Education

Minimum: Bachelor’s degree in Computer Science / Electronics / Electrical Engineering, or a related field.
Preferred: Experience working in Regulated industries is a plus.

The base pay for this position is

$86,700.00 – $173,300.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Product Development

DIVISION:

CRM Cardiac Rhythm Management

LOCATION:

United States > Sylmar : 13150 Telfair Avenue

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

MEDICAL SURVEILLANCE:

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

Senior Software Engineer