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 The duties related to the Sr Reliability Engineer role requires advance knowledge and experience in Medical Device industry to perform risk assessments, ensuring product risks are captured and maintained, perform design quality reviews, support potential product quality issues in released product portfolio. It also encompasses all aspects of a medical device’s lifecycle such as design, manufacturing, distribution and obsolescence. The diversity of duties ranges from performing quality impact assessments, addressing potential product quality issues, technical writing (Risk Management Review report, Design Failure Mode Effect Analysis, and other related technical documentation) to creative and critical thinking, working with diverse teams and leading in resolving quality issues and process improvements. The duties are complex as depending on the complexity of the issues, all duties and projects are often performed in parallel. The products that the Employee will work on support the Core Surgical Innovations (CSI) product portfolio within the Medical Surgical operating unit. The specific product portfolio includes different stapling products with complex design technologies. The employee will be the lead design quality engineer for one of the many stapling products within the product portfolio. Extensive and deep knowledge in understanding product design helps to address quality issues, assess risks associated with the product and ensure product reliability standards are met. The Employee’s work will have an immediate impact on the CSI product Stapling portfolio and business performance that there are significant continuous improvement projects, product/process changes to be implemented to fulfill the market requirements. Extensive work associated to perform product quality assessment, review and approval of technical documentations related to engineering changes, perform root cause investigations to address quality issues, update and maintain risk management files, to ensure quality standards and business unit goals are met. Other type of activities involve review and analyzing product complaint trends to be aware of trends in Medical device industry. The duties that Employee performs are vital in ensuring products of the highest quality is being provided to patients.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees