SYSTEM PROCESS ENGINEER

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, 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 is 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. Summary In this position, you will be managing technical activities and projects in the monitor manufacturing area. You’ll collaborate with the manager for the management of HW Monitor's technical activities and coordinate complex projects within the scope of your technical skills. Performing validations and contributing to the continuous improvement program of production and products is also part of your activities. #Thisiswhere you can leverage your technical expertise in production processes and products, helping Baxter in saving and sustaining lives. What you'll be doing Coordinate projects and activities that require technical involvement, in agreement with the Manufacturing Engineering Manager, defining the times and resources allocated to the various activities. Collaborate with R&D, System Support, and Quality for the management of the projects. Ensure the Design Transfer process from R&D to Manufacturing. Conduct production process validation activities in accordance with current company procedures. The activity also includes the proposal of improvements to the production processes, if necessary, during validation or sustaining activities. Analyze specific technical problems related to modifications, industrialization, functional tests, and commissioning production of individual components/mechanical subassemblies/complex benches, defining solutions and collaborating with the other corporate bodies involved. Guarantee active support in the industrialization phase of the product/production process starting from the editorial staff of User Requirement/Detailed Design and following the activities of FAT, SAT, Review, and validation. Ensure the availability of the technical documentation in accordance with company procedures and applied regulations. Support QA Team in activities related to investigations, CAPA, and Non-Conformities. Train production personnel for production processes and procedures, if needed. What you’ll bring Master’s degree in engineering (Mechanical, Automation, Electrical, Biomedical, Chemical…) 5+ years’ experience in validation or in production engineering field better if within large companies in the manufacturing and/or pharmaceutical sectors. Knowledge of complex electromedical production processes (better if dialysis equipment). Team working attitude and problem-solving skills. Green Belt certification is a plus. Fluent Italian and English knowledge (written and spoken). #J-18808-Ljbffr