Quality Engineer II

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About the role

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 Quality function partners with Research & Development and Operations teams to ensure medical devices are designed, developed, and maintained in compliance with applicable quality system regulations, risk management requirements, and international standards. The team provides quality engineering leadership throughout the product lifecycle, supporting design controls, verification and validation activities, risk management, product transfers, regulatory compliance, and continuous quality improvement initiatives. This position is based in Hyderabad, India and follows a Flex work arrangement. No travel is required. As a Quality Engineer II, you will provide design quality engineering support for medical device product development and sustaining engineering activities. The role is responsible for facilitating the application of design controls, risk management, design verification and validation, and regulatory compliance activities while partnering with cross-functional teams throughout the product lifecycle. Primary Responsibilities • Review new and modified product design documentation for quality characteristics, including manufacturability, serviceability, testability, reliability, and product requirements. • Ensure product development projects and design changes comply with FDA Quality System Regulations, European Union Medical Device Regulation (EU MDR), and internal quality requirements. • Partner with cross-functional teams to develop and maintain risk management documentation, including Risk Management Plans, Hazard Analyses, Design Failure Mode and Effects Analysis (DFMEA), and Risk Management Reports in accordance with ISO 14971. • Support design verification and validation activities through development and review of plans, protocols, reports, testing strategies, and compliance assessments. • Review Design History Files (DHF) and Technical Files for compliance with applicable regulations, standards, and quality requirements. • Support successful transfer of products into manufacturing through process validation activities, including Process Failure Mode and Effects Analysis (PFMEA), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). • Develop quality system templates, training materials, and guidance related to design controls, risk management, quality system regulations, and applicable standards. • Participate in internal and external audits and provide quality engineering guidance across project teams and organizational functions. Required Qualifications • Bachelor's degree in Mechanical Engineering with 5+ years of overall experience, including 3+ years of quality engineering experience in medical device, regulated manufacturing, or healthcare industries. • Experience with medical device Design Controls, Risk Management, and product development activities. • Experience supporting ISO 14971 risk management activities, including Risk Management Plans, Hazard Analyses, and Design Failure Mode and Effects Analysis (DFMEA). • Knowledge of FDA Quality System Regulation, ISO 13485, EU MDR, IEC 60601, 21 CFR Part 820, and 21 CFR Part 11. • Experience using statistical tools and methodologies, including Minitab, sampling plans, hypothesis testing, Analysis of Variance (ANOVA), Gauge Rep

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