System Process Engineer

3 settimane fa

Medolla, Emilia-Romagna, Italia Baxter A tempo pieno

Job Summary
Vantive, a new company built on Baxter's legacy, is revolutionizing kidney care and other vital organ support. We're seeking a skilled System Process Engineer to manage technical activities and projects in the monitor manufacturing area.

About the Role
As a System Process Engineer, you will collaborate with the Manufacturing Engineering Manager to coordinate complex projects within your technical skills. You'll perform validations, contribute to the continuous improvement program of production and products, and leverage your technical expertise to help Baxter save and sustain lives.

Key Responsibilities
Coordinate projects and activities that require technical involvement, defining times and resources allocated to various activities.
Collaborate with RD, System Support, and Quality for project management.
Ensure Design Transfer process from RD to Manufacturing.
Conduct production process validation activities in accordance with current company procedures.
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 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 activities of FAT, SAT, Review, and validation.
Ensure the availability of technical documentation in accordance with company procedures and applicable regulations.
Support QA Team in activities related to investigations, CAPA, and Non-Conformities.
Train production personnel for production processes and procedures, if needed.

Requirements
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).

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