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Michael Page
Contratto a tempo indeterminato
    Multinational Company Support the Software Team in clarifying and defining software requirements from customer needs, instrument manufacturer, service, marketing and assay R&D. Design and development of software and firmware for diagnostics instrumentation and related. Define, review and update software specifications and design details derived from user requirements. Define technical documentation related to the software and firmware under development or maintenance. Contribute actively to troubleshoot the released and under development software and firmware. Investigate on anomalous and/or uncommon situations. Edit, review and perform software verification/validation/unit test plans and protocols. Interact with the other development areas within the Team ("Hardware" and "Assay Integration"), in order to investigate the feasibility of proposed implementations and solutions. Interact with other Company functions, in order to provide team's expertise and support to problem solving. Ensure compliance with the Quality Management System, the Company Policies and the Corporate Procedures. Responsible for performing assigned tasks in accordance with applicable safety regulations and instructions, as well as correcting unsafe work habits and practices and/or bringing to the attention of the supervisor any practice or condition that may be detrimental to the safety and health of the employees. Perform other duties as assigned. Master's Degree in Computer Science, Engineering of Computing Systems 5-10 year experience in computer programming is required Previous experience in IVD (In Vitro Diagnostics) and/or highly regulated FDA environments and biotechnology industry experience is highly appreciated Apply knowledge of computing systems and software structure. Knowledge of C#, Microsoft Visual Studio and Team Foundation Server or equivalent is mandatory Knowledge of embedded systems ù Knowledge of optics (light sources, detectors and routing) is desirable Knowledge of heat (generation, transport, absorption and modeling) is desirable Knowledge of Polymerase Chain Reaction and/or molecular biology principles is desirable Knowledge of GMP (Good Manufacturing Practice) is appreciated Seasoned experience using Microsoft Office package. Test software applications and systems Create documentation, manuals and detailed sets of instructions including algorithms in pseudo code and computer programs Fluent spoken and written Italian and English
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