Global Software Development Engineer Immuno - Saluggia, Italy - ITA 2022-040

Job Title

Global Software Development Engineer Immuno

Job Facts

Organizational Area
Italy and UK Branch
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 2022-040

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 (“Consumables", “Hardware” and “Assay Integration”), with Project Management and Device Lead, 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
  • 2-3 years experience in a similar role
  • Previous experience in IVD (In Vitro Diagnostics) and/or highly regulated FDA environments and biotechnology industry experience is highly appreciated
Technical Competencies
  • Knowledge SW Life cycle (FDA guidance - EN 62304)
  • Knowledge change management process
  • Knowledge of requirements engineering approach (nice to have)
  • 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
  • Focus on results
Fluent spoken and written Italian and English
Travel Availability
Travels may be required
Relocation Availability
Training Required

Induction Program Once Hired


We Offer You

As for Company Policy