System Development & Integration - Software Engineer - Saluggia, Italy - ITA 2016-004

Job Title

System Development & Integration - Software Engineer

Job Facts

Organizational Area
Country / State
Place of work
Home/Office based
Office based

Professional Family: 

  • R&D - SD&I
Reporting To
Software Development Manager

Kind of contract

Full Time / Part Time
Full Time
Permanent / Temporary
Job ID
ITA 2016-004

Job Scope

Your Mission

To provide a valuable operative and documentary contribution to the Team in accomplishing Software design and test activities, related to development of new instruments and improvement of existing instruments, through a professional, quality-driven and proactive attitude, with the target of building a solid Corporate know-how and in order to transfer to DiaSorin Customers the best quality in products and services.

Main Responsibilities

Your Contributions
  • Define, review and update software requirements (high-level and low-level) deriving from higher level requirements, from market feed-back or from regulatory/safety requirements
  • Review the associated software specifications
  • Interact with the other development areas within the Team (“Hardware” and “Assay Integration”), as per the joint development/improvement tasks
  • Manage software installations aimed at software testing activities
  • Edit, review and perform software verification/validation plans
  • Contribute actively to troubleshooting and bug fixing activities with the instrument Development Partners
  • Investigate on anomalous and/or uncommon situations
  • Interact with other Company functions, in order to provide team’s know-how and support to problem solving
  • Ensure compliance with the Code of Ethics, the Quality Management System, the Company Policies and the Corporate Procedures

Qualifications Experience Personal Strengths Mobility

Master’s Degree
Engineering, Physics, Informatics, Mathematics
  • 1-2 years experience in a technical field is a plus
  • Previous experience in IVD (In Vitro Diagnostics) and/or highly regulated FDA environments and biotechnology industry experience is highly appreciated
Technical Competencies
  • Knowledge of GMP (Good Manufacturing Practice) is appreciated
  • Seasoned experience using Microsoft Office package
  • Basic level of programming skills
  • Accuracy, comprehension of technical issues
  • High problem-solving and decision-making capability
  • Effective analytical skills
  • Interdisciplinary thought and quality awareness
  • Well organized, ability to work well independently as well as part of a team
  • High commitment and willingness to learn
  • Positive, proactive and open-minded attitude
  • Strong commitment
  • Willingness to learn
  • Focus on results
Fluent spoken and written Italian and English
Travel Availability
Periodical travels may be required, based on ongoing project phases (max. typical: a few days every 1-3 months, typically in Europe)
Relocation Availability
Not required
Training Required

Not required


We Offer You

As per local and Company requirements.