Staff SW Test Engineer

Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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 a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

At Lingo, we’re building a groundbreaking health platform that combines continuous biosensor data, real-time analytics, and personalized insights to help people live fuller, longer, and healthier lives. Our systems ingest millions of sensor readings daily, powering experiences for consumers and partners worldwide, with the reliability and scalability of cloud-native, enterprise-grade platforms.   We are seeking a Staff Software Test Engineer to lead verification and validation efforts across our cloud, and mobile platforms within a regulated medical device environment. This role is based in Hyderabad, India, and plays a critical role in ensuring product quality, regulatory compliance, and scalable delivery. What You’ll Work On  Own and execute end‑to‑end software verification for cloud services, mobile applications, and connected devices, ensuring quality throughout the development lifecycle Translate product and technical requirements into comprehensive verification strategies, test plans, test cases, and execution plans Develop, maintain, and continuously improve verification plans, protocols, and reports in compliance with FDA 21 CFR, ISO 13485, IEC 62304, and related standards Partner closely with product managers, architects, developers, and quality teams to ensure requirements are testable, traceable, and aligned with verification strategies Support risk management activities, including risk analysis, defect triage, impact assessments, and root‑cause investigations Participate in design reviews and verify design inputs and outputs meet regulatory and quality expectations Design and implement scalable manual and automated testing strategies spanning functional, integration, system, and regression testing Drive continuous improvement across verification processes, tools, metrics, and automation coverage Mentor and guide junior test engineers, promoting strong engineering discipline, automation best practices, and regulatory excellence Required Qualifications Bachelor’s degree in software engineering or a related field, or equivalent practical experience 10+ years of experience in software verification and quality engineering 3+ years of experience in medical device software development under FDA 21 CFR 820, ISO 13485, and IEC 62304 Strong expertise in medical device V&V, including defect management and requirements traceability Demonstrated experience identifying and implementing test automation opportunities across mobile, web, API, or similar platforms Excellent analytical, communication, and documentation skills, with a collaborative mindset Hands‑on experience building scalable automation frameworks (e.g., PyTest, Playwright, Jest, REST Assured) Proficiency in Python, JavaScript, or TypeScript, with the ability to create reusable automation tools Preferred Qualifications Background in healthcare or other regulated industries Solid understanding of SDLC, QA methodologies, and