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Abbott

Sr. Software Engineer

Abbott, Los Angeles, California, United States, 90079


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 opportunity for a

Sr. 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 Understand product requirements and use cases, and work on verification applications for Cardiac Rhythm Management (CRM) remote care, including but not limited to technical requirements development, identifying test strategy, development of test design, test cases, test procedures and scripts, and test execution. Independently develop, debug and maintain automated test procedures. Train/mentor others on the teams. Participate in and support the implementation, development, enhancements, and modifications to software test scripts and procedures. Debug, troubleshoot, and isolate software problems and offer strategic solutions, analysis, and advice regarding identified issues for future development. Identify parameters, structure, and critical test components. Write, update, or execute test design, test cases, as well as test procedures (automated, semi-automated or manual) and analyze and report test results. Create test scenarios to simulate clinical workflows related to Class III and Class II medical devices such as ICDs, Pacemakers and Heart Monitors. Contribute to and support writing, updating, developing and maintaining Hazard/Risk/Cyber Security analysis specifications and cybersecurity testing. Working from requirement specifications, develop, maintain, and update design/test protocols. Present at design reviews; document and resolve issues. Perform analysis and defect repair of one or more issues in the applications, as well as perform root cause analysis and identify corrective and preventive actions to address current and future issues. Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. Required Qualifications Bachelor's Degree in Software Engineering, Computer Science, or a related engineering field, or an equivalent combination of education and work experience. Minimum 6 years

of progressively more responsible work experience in a range of software engineering disciplines using a variety of programming methods. Preferred Qualifications Experience with C# and/or Java is required. Experience with formal software development methodologies, and source code management is recommended. Experience with unit and integration-level testing and automated testing is recommended. Experience with testing software in the implantable medical devices domain is required. Ability to work in a highly matrixed and geographically diverse business environment. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitask, prioritize and meet deadlines in a timely manner. Strong organizational and follow-up skills, as well as attention to detail. Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:

www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at

www.abbott.com , on Facebook at

www.facebook.com/Abbott

and on Twitter @AbbottNews. The base pay for this position is

$83,600.00 – $167,200.00. 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:

Yes, 5 % of the Time

MEDICAL SURVEILLANCE:

Not Applicable

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

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