As a Senior Software QA Engineer II, you will : Own and lead the design and execution of verification strategies, including test plans, protocols, reports, and traceability matrices, in compliance with FDA, IEC 62304, and ISO 13485 requirements.Reports project status, tracks test metrics and ability to work on multiple projects and meet deadlines. Review and contribute to requirements and design documentation with a focus on quality, accuracy, completeness, and testability.Work with databases, APIs, and Linux environments to validate data integrity, system behavior, and workflow accuracy.10+ years of software QA experience, with 3+ years in medical device or FDA-regulated software development.Experience leading Verification test efforts for medium to large size projects.Experience supporting regulatory submissions and audits. Excellent analytical and problem-solving skills with the ability to work independently. Effective written and verbal communication skills; strong attention to detail. Hands-on experience with MySQL, Linux, and working in Agile environments. Ability to quickly learn new tools, applications, and technologies. Proven ability to act as a quality advocate within cross-functional teams, influencing design and development decisions to strengthen overall product quality.Familiarity with ISO 14971 (risk management) and IEC 62304 a plus.Experience with regression test automation a plus. At iRhythm, you'll have the opportunity to grow your skills and your career while impacting the lives of people around the world. Together, we are reimagining the way cardiac arrhythmias are diagnosed. We need curious problem solvers like you. With opportunities remotely, at our office, in manufacturing, and in locations across the globe, this is your chance to meaningfully shape the future of cardiac health, our company, and your career.
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Software Engineer • WorkFromHome, Qatar