Senior Quality Software Engineer

Job ID: 31156548Posted: Posted 5 Days AgoStart Date: 2026-08-03Location: United States - Illinois - Lake Forest, United States of AmericaTime Type: Full timeAbbott 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 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:Job TitleSr. Software Engineer, QualityWorking at AbbottAt 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 of which you dream.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 contributionTuition 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 The Sr. Software Engineer, Quality acts as a bridge between technical and non-technical stakeholders, translating software quality, validation, compliance, and system requirements into clear, actionable information for business partners including Sales, Commercial, Quality, Operations, and other cross-functional teams.This role can be in any of our Abbott location in the United States. This is an onsite role. MAIN PURPOSE OF ROLECommunicates complex software quality, validation, and regulatory requirements in a clear and practical manner to technical and non-technical audiences, driving alignment and informed decision-making across functions.Reviews documentation for accuracy, clarity, consistency, completeness and compliance for multiple projects. Plans and performs assignments with a wide degree of difficulty.Analyzes data, procedures, and requirements with consideration given to financial and business outcomes.Coordinates activities across impacted groups. Accepts ownership and responsibility for decisions.Effectively engages team members and provides guidance to various functions, other professionals, and technicians.MAIN RESPONSIBILITIESReviews pre-defined deliverables/activities as identified in software quality assurance (SWQA) Non-Product Quality Process and/or SWQA Product Quality Process/project plan or equivalent project plan.Applies basic 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 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.Assists with supplier assessments and evaluations to assure products and services meet quality requirements. May evaluate vendor capabilities to provide required products or services.Education and Experience You’ll BringEducation Level Bachelor's Degree in computer science, software engineering, or a closely related discipline or an equivalent combination of education and work experience. Master’s degree preferredExperience/Background ExperienceMinimum 4 years related work experience in Quality or a related field.SBM, Ariba or similar platformMS SuiteKnowledgeable of FDA, Quality System Regulations (QSR), Medical Device Directive, ISO guidelines and 21 CFR Part 11.Project experience in software testing practices, methodologies and techniques, particularly in testing medical devices or experience leading test engineer team is a plusApply NowLearn more about our health and wellness benefits, which provide the security to help you and your family live full lives: 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 , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.The base pay for this position is $78,000.00 – $156,000.00In specific locations, the pay range may vary from the range posted.JOB FAMILY:Operations QualityDIVISION:AVD VascularLOCATION:United States > Lake Forest : CP01ADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 10 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: is the Law link - Espanol: