R&D Therapy System Engineer

Vantive: A New Company Built On Our LegacyBaxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.Job DescriptionSummaryThe Therapy System Engineer will execute system engineering tasks during the life cycle of an active medical device, from the design to development up to the sustaining. You will collaborate with multidisciplinary teams and work in a global, dynamic, and fast-paced environment.What you'll be doingJoin Therapy Systems Engineering efforts for a complex, active medical device.Collaborate to the development and integration of an active medical device.Collaborate to the development and implementation of therapy related functionalities. Collaborate to the maintenance of product requirements, design description and other technical documentation.Collaborate to the development of controls trough model-based methodologies.Collaborate to maintain the product Design History File (DHF) of an active medical device.Collaborate in Risk Management activities to ensure that design and process shortcomings are identified and appropriately addressed..What you'll bringUniversity degree in Scientific Engineering.Matlab Simulink State flow proven knowledge.Embedded Control Loop expertiseWelcome are experiences on product design, development, and/or testing in the area of medical device.Able to communicate effectively within an international and multi-site environment.Welcome is experience related to regulatory and standards (ISO 13485, IEC 62366, IEC 60601.1 IEC 60601.2.16, ISO 14971.21CFR801, MDD, MDR)Fluent in English both verbally and in writing