Principal Enterprise Software Test Engineer

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life The Acute Care Monitoring (ACM) Research & Development organization develops software and technology solutions that support patient monitoring and respiratory interventions across the continuum of care. The software verification and validation function is responsible for ensuring product quality, reliability, safety, and regulatory compliance through comprehensive test strategy development, test automation, verification and validation activities, and continuous quality improvements for medical device software products. This position is based in Hyderabad, India and follows a Flex work arrangement. No travel is required.As a senior software verification and validation professional, you will lead verification and validation activities for medical device software products across multiple programs. The role focuses on test strategy development, test automation, software quality assurance, regulatory compliance, and cross-functional collaboration to ensure safe, effective, and high-quality software releases for Acute Care Monitoring products. Primary Responsibilities Lead software verification and validation activities across multiple medical device software programs and serve as test lead for RPE initiatives. Design, develop, and execute verification and validation strategies using manual and automated testing methodologies. Develop and enhance test automation frameworks for desktop, web, mobile, and embedded software applications. Review software requirements, test designs, and test scripts to ensure comprehensive verification of product functionality and quality requirements. Collaborate with global cross-functional Agile teams throughout requirements, design, implementation, verification, and release activities. Support non-product tool validation (NPTV), defect analysis, risk assessments, static code analysis, and quality assurance activities. Mentor verification and validation engineers, promote testing best practices, and support continuous process improvements. Ensure compliance with medical device software standards, quality requirements, and project performance objectives. Required Qualifications Bachelor's degree OR Master's degree in Computer Science, Biomedical Engineering, Biotechnology, Electronics Engineering, Electrical Engineering, or related technical discipline with 15+ years of experience in software verification and validation, including 2+ years in medical device, medical IT, or other regulated industries.