R&D Therapy System Principal Engineer

Social network you want to login/join with: R&D Therapy System Principal Engineer, Medolla Client: Baxter Location: Job Category: Other - EU work permit required: Yes Job Reference: 807e73434b29 Job Views: 2 Posted: 06.05.2025 Expiry Date: 20.06.2025 Job Description Vantive: A New Company Built On Our Legacy Baxter 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, but also offer meaningful work to those who join us. At Vantive, you will become part of a community of focused, courageous individuals who don’t settle for mediocrity. We are driven to 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. Summary The R&D Therapy System Principal Engineer will execute system engineering tasks throughout the lifecycle of an active medical device, from design and development to sustaining. This role involves collaboration with multidisciplinary teams in a global, dynamic, and fast-paced environment. What you'll be doing Join Therapy Systems Engineering efforts for a complex, active medical device Understand human-factor engineering to translate user needs into system requirements Develop and maintain product requirements, design descriptions, and other technical documentation Collaborate to maintain the product Design History File (DHF) of an active medical device Participate in Risk Management activities to identify and address design and process shortcomings What you'll bring University degree in Engineering or relevant experience in medical device R&D 5 years of experience in product design, development, and testing of medical devices Strong understanding of System Design and Therapy development Experience with design for manufacturing and reliability is preferred Effective communication skills in an international, multi-site environment Experience with regulations and standards (ISO 13485, IEC 62366, IEC 60601.1, IEC 60601.2.16, ISO 14971, 21CFR801, MDD, MDR) is welcome Fluent in English, both verbal and written J-18808-Ljbffr

Location: medolla, IT

Posted Date: 5/11/2025