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Archiviertes Projekt - Senior Software Engineer

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Juni 2020

Juni 2020


auf Anfrage




Senior Software Engineer - Medical Devices

Tasks & Responsibilities:

* Specify, design, develop, code, master the software release and maintain the software for the client products
* Collaborate with internal and external software teams for development, integration of the product with other software solutions
* Setup 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 standards
* Participate to verification and validation effort, ensure efficient, robust and high coverage test strategy
* Collaborate with Quality and Regulatory team for impact analysis, software risk or quality assessment and provide support in case of audit
* Make 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 plus
* Knowledge in SW dev processes according Medical Devices Regulation and standards in US and EU
* Relevant experience in Real Time Systems, Embedded targets, RTOS
* Relevant experience in windows technologies, .NET framework, windows drivers model, WPF, Winforms, WCF
* Relevant 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 Files
* Experience with designing software products in an FDA or other regulated industry

Understand Change Control, Design Control and Software Development Life Cycle management

Familiar with concepts of design input, design output, traceability and risk analysis

Experience 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: ASAP
* Location: Lausanne (Remote until Covid Restrictions are lifted)
* Language: Fluent in English, French is a big plus
* Project Duration: min. 6 Months


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