Requirements: English
Company: TN Italy
Region: Province of Modena , Emilia-Romagna
Social network you want to login/join with: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, but 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 dont settle for mediocrity. 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.SummaryIn this position, you will manage technical activities and projects in the monitor manufacturing area.Youll collaborate with the manager to oversee HW Monitor''s technical activities and coordinate complex projects within your technical scope. Performing validations and contributing to the continuous improvement program of production and products are also part of your responsibilities.#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 requiring technical involvement, in agreement with the Manufacturing Engineering Manager, defining the timelines and resources allocatedCollaborate with R&D, System Support, and Quality for project managementEnsure the Design Transfer process from R&D to ManufacturingConduct production process validation activities following current company procedures, including proposing improvements during validation or sustaining activitiesAnalyze specific technical problems related to modifications, industrialization, functional tests, and commissioning of components, defining solutions and collaborating with involved departmentsSupport the industrialization phase of products and production processes, from User Requirements/Detailed Design to FAT, SAT, review, and validation activitiesEnsure the availability of technical documentation in accordance with company procedures and regulationsAssist QA in investigations, CAPA, and Non-ConformitiesTrain production personnel on processes and procedures as neededWhat youll bring5+ years of experience in validation or production engineering, preferably within large manufacturing or pharmaceutical companiesKnowledge of complex electromedical production processes, ideally dialysis equipmentTeamwork attitude and problem-solving skillsGreen Belt certification is a plusFluent in Italian and English, both written and spoken#J-18808-Ljbffr