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Process Engineering Specialist

3 mesi fa


Medolla, Emilia-Romagna, Italia Baxter A tempo pieno

Vantive: A New Company Built On Our Legacy

Baxter is embarking on a transformative journey to establish our ~$5B Kidney Care segment as an independent entity. Vantive* will leverage our nearly 70-year history in acute therapies and dialysis services to deliver exceptional care to our patients. We believe that Vantive will not only enhance our leadership in the kidney care sector but also provide fulfilling opportunities for those who join our mission.

At Vantive, you will be part of a dedicated community of professionals who are focused, courageous, and committed to excellence. Each team member is motivated to make a positive impact on patients' lives globally. Together, we are set to revolutionize kidney care and support for other vital organs.

*The proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) is subject to the fulfillment of customary conditions.

Position Overview

In this role, you will oversee technical initiatives and projects within the monitor manufacturing sector.

You will collaborate closely with the Manufacturing Engineering Manager to manage the technical activities related to HW Monitor and coordinate intricate projects aligned with your technical expertise. Your responsibilities will also include conducting validations and contributing to the ongoing improvement initiatives for production and products.

#Thisiswhere you can apply your technical knowledge in production processes and products, assisting Baxter in our mission of Saving and Sustaining lives.

Key Responsibilities

  • Coordinate projects and activities requiring technical engagement, in alignment with the Manufacturing Engineering Manager, while defining timelines and resources for various tasks.
  • Collaborate with R&D, System Support, and Quality teams for effective project management.
  • Ensure the successful transition of designs from R&D to Manufacturing.
  • Conduct validation activities for production processes in accordance with established company protocols, including proposing enhancements during validation or ongoing support activities.
  • Analyze specific technical challenges related to modifications, industrialization, functional testing, and the commissioning of individual components/mechanical subassemblies/complex benches, defining solutions and working with relevant corporate teams.
  • Provide active support during the industrialization phase of products and production processes, starting from the User Requirement/Detailed Design phase and continuing through FAT, SAT, Review, and validation activities.
  • Ensure the availability of technical documentation in compliance with company procedures and applicable regulations.
  • Assist the QA Team with investigations, CAPA, and Non-Conformities as needed.
  • Train production staff on processes and procedures as required.

Qualifications

  • Master's degree in engineering (Mechanical, Automation, Electrical, Biomedical, Chemical, etc.).
  • 5+ years of experience in validation or production engineering, preferably within large manufacturing or pharmaceutical organizations.
  • Familiarity with complex electromedical production processes, particularly in dialysis equipment.
  • Strong teamwork orientation and problem-solving capabilities.
  • Green Belt certification is advantageous.
  • Proficiency in both Italian and English (written and spoken).