System Process Engineer

1 settimana fa


Medolla, Italia Baxter A tempo pieno

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.SummaryIn 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 coordinates complex projects within the scope of your technical skills.Performing validations and contribute 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 doingCoordinate projects and activities that require technical involvement, in agreement with the Manufacturing Engineering Manager, defining the times and resources allocated to the various activitiesCollaborate with R&D, System Support e Quality for the management of the projectsEnsure the Design Transfer process from R&D to ManufacturingConduct 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 involvedGuarantee active support in the industrialization phase of the product/production process starting by the editorial staff of User Requirement/Detailed Design and following the activities of FAT, SAT, Review and validationEnsure the availability of the technical documentation in accordance with company procedures and applied regulationsSupport QA Team in activities relates to investigations, CAPA and Non-ConformitiesTrain production personnel for production processes and procedures, if neededWhat you'll bringMaster'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 sectorsKnowledge of complex electromedical production processes (better if dialysis equipment)Team working attitude and problem-solving skillsGreen Belt certification is a plusFluent Italian and English knowledge (written and spoken)


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