Senior Software Engineer

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Senior Software Engineer - Medical Devices Tasks & Responsibilities:Specify, design, develop, code, master the software release and maintain the software for the client productsCollaborate with internal and external software teams for development, integration of the product with other software solutionsSetup testing platform, issues Investigations, root cause analysis, Bug Correction and sustaining activities. Continuous improvement of software quality, reliability and safety.Author, improve or review software documentation (including specifications, design and verification documents) by focusing on quality, reliability and safety of BINJ software products, as well as compliance with relevant standardsParticipate to verification and validation effort, ensure efficient, robust and high coverage test strategyCollaborate with Quality and Regulatory team for impact analysis, software risk or quality assessment and provide support in case of auditMake propositions and contribute to the R&D process optimization

Your Profile / Experience:

Proficiency in C# / VB .Net, SQL with expertise in multitasking, multithreading, object oriented programming,Proficiency in C, C++ is a plusKnowledge in SW dev processes according Medical Devices Regulation and standards in US and EURelevant experience in Real Time Systems, Embedded targets, RTOSRelevant experience in windows technologies, .NET framework, windows drivers model, WPF, Winforms, WCFRelevant experiences in software development and modular architecture design (UML, SOA, design patterns)Relevant experience in Source version control (GIT), Continuous integration (Jenkins, Teamcity), Bug tracking systems, Unit testing frameworks (CppUnit, NUnit,, LDRA),Experience with automated testing frameworks,Strong documentation and writing skills and ability to follow Quality and Regulatory requirements, prepare DHF and Technical FilesExperience with designing software products in an FDA or other regulated industryUnderstand Change Control, Design Control and Software Development Life Cycle managementFamiliar with concepts of design input, design output, traceability and risk analysisExperience with class II or III medical devices and/or with medical software standards (i.e. IEC 62304 & FDA related guidance) is a big plus Project Details:Start Date: ASAPLocation: Lausanne (Remote until Covid Restrictions are lifted)Language: Fluent in English, French is a big plusProject Duration: min. 6 Months Interested? Apply online or contact us at +41 (0)44 588 2649-Sthree Switzerland is acting as an Employment Business in relation to this vacancy.