At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all You ll lead with purpose breaking down barriers to innovation in a more connected compassionate world A Day in the Life Collaborating with cross-functional teams to develop comprehensive product risk management files including the risk management plan Hazard Analysis DFMEA and risk management report adhering to ISO 14971 standards Responsible for maintaining highest standards of product reliability and patient well-being through gather and analyze data write reports and communicate with regulatory agencies on ensuring product safety Responsibilities may include the following and other duties may be assigned Capability to conduct thorough reviews of new and modified product design documentation assessing quality characteristics such as manufacturability serviceability testability reliability and compliance with product requirements Subject matter expert in risk management for designated medical device products or platforms Ensuring compliance with FDA Quality System Regulations EU MDR ISO 13485 ISO 14971 IEC 60601 and other relevant industry standards during product development and changes Reviewing Design History Files and Technical Files to ensure alignment with applicable requirements Collaborate with cross-functional teams to gather and analyze data related to the performance and safety of medical devices and independently develop Periodic safety update plan and reports Partner with regulatory affairs and medical experts to ensure accurate and timely submission of PSURs to regulatory authorities Continuously monitor and stay updated with evolving safety regulations and guidelines to ensure PSUR compliance Familiar with Literature review PMCF IMDRF coding CAPA and NCMR Hands on experience in signal evaluation trending and reports preliminary code reviews for the product complaints on periodic basis Delivering presentations on project status and issues to the QA organization and providing training to other departments on relevant procedures and policies Participating in audits and demonstrating the ability to effectively contribute as a team player in various roles including contributor subject matter expert leader and facilitator Provide Quality support to facilitate resolution of product complaints and or safety issues Previous experience working in a cross-functional team environment Familiar with statistical software tools Minitab Develop templates and trainings based on the quality system regulations applicable standards and guidance Independently review all deliverables to ensure compliance with development process and the standard Demonstrates ability to effectively play multiple roles on a cross-functional team including contributor subject matter expert leader facilitator Hands-on experience on complaints analyis Post market surveillance Design Controls for Medical Devices Required Knowledge and Experience B E or B Tech in Mechanical Biomedical Engineering Minimum 4-6 years of quality engineering experience or equivalence and overall 6-8 years of experience Familiar with ISO 9001 ISO 13485 ISO 14971 IEC 60601 21 CFR part 820 21 CFR part 11 EUMDR and product specific industry standards Working knowledge of and auditing experience to the FDA Quality System Regulation ISO 13485 and the Medical Device Directive Good verbal and written communication skills Understanding of post-market surveillance processes and adverse event reporting Knowledge of risk management principles and hazard analysis in the context of medical devices Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position but they are not an exhaustive list of all the required responsibilities and skills of this position Benefits Compensation Medtronic offers a market-competitive salary and flexible Benefits Package A commitment to our employees lives at the core of our values We recognize their contributions They share in the success they help to create We offer a wide range of benefits resources and competitive compensation plans designed to support you at every career and life stage About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions Our Mission to alleviate pain restore health and extend life unites a global team of 95 000 passionate people We are engineers at heart putting ambitious ideas to work to generate real solutions for real people From the R D lab to the factory floor to the conference room every one of us experiments creates builds improves and solves We have the talent diverse perspectives and guts to engineer the extraordinary

📌 Quality Engineer Ii (Telangana)
🏢 Medtronic
📍 Telangana