System Development & Integration
DiaSorin S.p.A.
3 gg fa

Job Facts

Legal Entity DiaSorin S.p.A. Saluggia VCItaly Organizational Area Corporate Country / State Italy Place of work Saluggia Home / Office based Office based

Professional Family :

  • Research and Development
  • Reporting To Software Development Manager

    Kind of contract

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

    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.

    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

    You Education Master’s Degree Specialization Engineering, Physics, Informatics, Mathematics Experience

  • 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
  • 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
  • Languages 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

    We Offer You

    As per local and Company requirements.

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