Job Description

We anticipate the application window for this opening will close on - 17 Jan 2025. 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 You would be joining our Product Development Organization as a Senior Principal Development Engineer responsible for the Verification Strategy, Requirement Decomposition, and Specification Development for our robotic projects in development. To us, Verification is not just the last step on the path to commercialization; this role becomes an integral core team member in the Concept phase of the project. You will be responsible for partnering with Systems Engineering, Marketing, the design teams, Quality and Project Management to drive meaningful product requirements, a robust design, and ultimately an efficient and effective verification strategy. Along the path to launch, you will become a technical contributor towards the success of the product and help establish best-practices and innovative approaches towards proving that our products meet the expectations of the Medtronic Mission. Location: North Haven, CT or Boston, MA The responsibilities of this role will include the following: Review and provide input to the development of product requirements. Review, provide input to and approve test methods. Design studies and experiments to gain confidence in meeting product requirements. Analyze test data. Author Engineering Analyses and Reports. Plan verification activities. Author Design Verification Protocols and Reports. Troubleshoot failures and make recommendations on design, test, or requirement improvements. Mentor junior engineers on all of the above. Champion continuous improvement projects, such as implementing new SOPs or WIs related to development engineering. Develop and drive a robust and efficient Design Verification strategy for product requirements. Author or review/approve Design Verification protocols and reports. Champion studies and/or activities that drive robust design, such as design of experiments, transfer function development, and simulations. Lead cross-functional failure investigations and analysis. Partner with System Engineering to develop, review and decompose product requirements. Represent the development engineering function on product development extended core teams. Mentor junior and senior development engineers working on your projects, and provide feedback on engineering reports, verification protocols, and verification reports. Liaison with Reliability, Compliance (60601), Hardware (Electrical and Mechanical), and Software teams for your projects. Support the development of regulatory submissions for your projects. Support QMS and/or DHF audits as the development engineer SME on those projects. Support changes made to your projects post-launch. Performs technical planning, system integration, verification and validation, evaluates alternatives including cost and risk, supportability and analyses for total systems. Analyses are performed at all levels of total system product to include: concept, design, fabrication, test, installation, operation, maintenance and disposal. Must Have: Minimum Requirements Bachelor’s Degree with 10+ years of engineering experience. OR An advanced degree with 8+ years of engineering experience. Nice to Have 8+ years of medical device development. Advanced degree in robotic engineering or another technical discipline. Industry experience with statistical methods and analysis of data to perform Design Verification. Experience with developing a product according to System Engineering principles. A strong understanding of Regulatory requirements for Design Controls and Design Verification. Industry experience with statistical analysis of data. Experience with robotics or electromechanical systems. Proven track record of contributing to medical devices of high complexity. Strong communication and interpersonal skills. 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. **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 90,000+ 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. It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. #J-18808-Ljbffr Medtronic

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