Fresenius Medical Care is the world’s leading provider of products and services for dialysis by offering innovative products and treatment concepts of the highest quality. We continuously want to improve the quality of life for our dialysis patients, worldwide and every day.

Our manufacturing plant in Palazzo Pignano specializes in producing bloodlines, operating around the clock with a dedicated workforce of more than 550 employees. Within this dynamic setting, our R&D departments play a pivotal role, ensuring that components and medical devices are correctly developed as per projects assigned in compliance with applicable regulations and internal procedures.

• Design components obtained by moulding and assembly of sub-parts. Skill in 3D cad design of plastic parts and related know how for manufacturing and assembly.
• Define and document medical devices development according to internal procedures and Design Control requirements
• Develop new product concepts collecting and analyzing input from clinical, marketing, literature and other sources
• Review and/or define new product and component requirements
• Review and/or define new component specification
• Develop test methods and equipment/fixtures
• Coordinate technical team for the realization and preparation of bill of materials, verification of adequate components availability, verification of supplier capacity, coordination with production to evaluate feasibility
• Support Risk Manager in Risk management activities
• Release and review project documentation (test protocols, test record and test reports)
• Generate intellectual property
• Support Product Interface documentation release acting Product Interface Manager role
• Support internal interfaces (Quality and Production department)
• Support material procurement and shipping requests
• Monitoring of suppliers concerning status of project and dealing with technical issues

Profile:

• Degree or similar education in biomedical / mechanical engineering discipline
• Advanced knowledge in technical drawing (3D, 2D cads)
• Knowledge of passive medical devices made in plastic materials
• Knowledge in plastic materials and relative manufacturing and assembly technologies
• English (level B1)
• Creo, Solidworks and Minitab
• Knowledge in computation analysis (es. CFD, FEA)
• Microsoft Office suite

• Design components obtained by moulding and assembly of sub-parts. Skill in 3D cad design of plastic parts and related know how for manufacturing and assembly.
• Define and document medical devices development according to internal procedures and Design Control requirements
• Develop new product concepts collecting and analyzing input from clinical, marketing, literature and other sources
• Review and/or define new product and component requirements
• Review and/or define new component specification
• Develop test methods and equipment/fixtures
• Coordinate technical team for the realization and preparation of bill of materials, verification of adequate components availability, verification of supplier capacity, coordination with production to evaluate feasibility
• Support Risk Manager in Risk management activities
• Release and review project documentation (test protocols, test record and test reports)
• Generate intellectual property
• Support Product Interface documentation release acting Product Interface Manager role
• Support internal interfaces (Quality and Production department)
• Support material procurement and shipping requests
• Monitoring of suppliers concerning status of project and dealing with technical issue