Global Consumables Development Engineer Immuno - Saluggia, Italy - ITA 2022-044

Job Title

Global Consumables Development Engineer Immuno

Job Facts

Organizational Area
Corporate
Country / State
Italy
Place of work
Saluggia
Home/Office based
Office based

Professional Family: 

  • R&D - SD&I
Reporting To
SD&I Immuno Consumables Development Manager

Kind of contract

Full Time / Part Time
Full Time
Permanent / Temporary
Permanent
Job ID
ITA 2022-044

Job Scope

Your Mission

The SD&I Immuno Consumables Development Engineer will make sure that the solid consumables are available and adequate for the immunology medical devices supplied by DiaSorin, to satisfy the needs of customers, assay developers, instrument and reagent manufacturers and servicing departments, through a professional, quality-driven and proactive attitude, with the target of building a solid Corporate know-how, in order to transfer to DiaSorin Customers the best quality in products and services.

Main Responsibilities

Your Contributions

Participate to define and update requirements and specifications for solid consumables to be used by DiaSorin immunology medical devices, in cooperation with internal corporate functions as well as suppliers.
Support technical tasks ongoing with development partners.
Support the evaluation of proposed technical solutions from a functional and documental perspective.
Perform the test activities, in order to ensure adequate consumables performance, reliability, serviceability, usability and to identify related weak points.
Cooperate with Immuno Assay Integration, Hardware and Software teams, to ensure proper integration of consumables with the DiaSorin immunology systems.
Cooperate with involved teams and suppliers to define qualification methods and control procedures for consumables.
Support the SD&I Immuno Consumables Development Manager in producing and monitoring project documents.
Perform 3rd level troubleshooting in regards to the released and under development consumables.
Ensure compliance with the Quality Management System, the Company Policies and the Corporate Procedures.

Qualifications Experience Personal Strengths Mobility

You
Education
Master’s Degree in Engineering, Materials Science or Physics
Specialization
-
Experience

from 1 to 4 years experience in a technical field is a plus, particularly if in the plastics field;
Previous experience in IVD (In Vitro Diagnostics) and/or highly regulated FDA environments is appreciated.

Technical Competencies

Knowledge of GMP (Good Manufacturing Practice) is appreciated
Seasoned experience using Microsoft Office package
Six sigma certification and Minitab knowledge will be a plus
Knowledge of CAD SW will be a plus

Skills

Accuracy, comprehension of technical issues
High problem-solving and decision-making capability
Effective analytical skills, in particular for root cause analysis
Interdisciplinary thought and quality awareness
Well organized, ability to work well independently as well as part of a team
High commitment
Positive, proactive and open-minded attitude
Willingness to learn
Focus on results

Languages
Fluent spoken and written English
Travel Availability
No
Relocation Availability
N/A
Training Required

Induction Program Once Hired

Benefits

We Offer You

As for Company Policy