Senior Software Quality Engineer – Design ControlsAbbott 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.This position works out of our Alameda, CA location in the Diabetes Care division where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions.
We're revolutionizing the way people monitor their glucose levels with our new sensing technology.The Senior Software Quality Engineer – Design Controls will be responsible for (but not limited to) the following:Participates as a lead member of the Software Quality Assurance (SWQA) team for Abbott Diabetes Care products to ensure medical device software is developed, tested and deployed in adherence to design control procedures.Engages cross-functionally with R&D teams (systems engineering, project management, software development and test) to review and approve DHF deliverables.Supports Agile teams as embedded design control SME throughout the product development and release cycle.Drives compliance to defect management process to ensure investigations are timely and thorough, risks/hazards are assessed, and fixes are implemented.What You'll Work OnCompletes software quality tasks in accordance with current Quality System Requirements.Works independently with objectives given by SWQA Manager.Can plan and coordinate own work according to higher-level project schedules.Reviews and provides lead guidance to the team regarding deliverables/activities as identified in project plans or equivalent documentation. Including System Specifications/Requirements documents, Verification Test Cases, Verification/Validation protocols, Trace Matrices and Verification/Validation Summary Reports for the Alameda site.Reports unexpected events, issues or software bugs which occur during verification/validation to project team and management.Coordinates the development and maintenance of departmental operating procedures to ensure compliance to relevant FDA, QSR, ISO guidelines, including 21 CFR Part 11 and Abbott Corporate requirements as they relate to the development, verification, validation, and maintenance of application in support of medical device software.Software Quality lead in various phases of the development lifecycle, as well as initiation of corrective and/or preventative action as it applies software development activities.Maintains schedule and drive to meet project schedule as aligned with project(s) goals.Will also estimate, plan, schedule and review own and others' work products and be accountable for the quality of those reviews and delivery on schedule.Considered SWQA compliance SME in support of external/internal audits.Required QualificationsBachelor's degree, or equivalent experience, in a scientific, technical, or engineering discipline.2 to 5 years' experience in Software Design Quality Assurance and/or Software Testing experience.Knowledge of FDA QSR, relevant ISO guidelines and 21 CFR Part 11. Has knowledge of Design Control and Risk Management requirements.Must have 1 - 3 years project experience in software testing practices, methodologies including Agile and techniques, preferably in testing medical devices and mobile applications.Preferred QualificationsMust have excellent oral and written communication skills.ASQ Certifications a plus.Medical Device experience strongly preferred.Cybersecurity, medical mobile applications or cloud computing experience preferred.The base pay for this position is $90,000.00 – $180,000.00.
In specific locations, the pay range may vary from the range posted.