My client is looking for a Software and Embedded Engineer.
What Youll Do:
- Specify design develop release and maintain the embedded and application software driving the contrast media injectors.
- Develop and maintain unit tests and automated tests
- Participate in verification and validation effort ensure efficient robust and high coverage test strategy
- Author improve or review software documentation (including specifications design and verification documents)
- Maintain and improve quality reliability and safety software products as well as compliance with relevant standards (IEC62304 FDA Guidelines)
- Make recommendations for design enhancements conduct feasibility studies and technical surveys
- Become an expert and reference person for the legacy software design
- Collaborate with other departments (such as Quality and Regulatory teams) for impact analysis software risk or quality assessment and provide support in case of audit
- Occasionally provide last level customer support
- Make propositions and contribute to the R&D process optimization
Requirements
What Youll Bring:
- You hold a Masters degree or PhD in Software Engineering Computer Science or Electrical Engineering
- You have at least 3 years of experience as a Software Engineer
- You possess a good understanding and proven experience working under software project methodologies (Waterfall VCycle or Agile)
- You have strong software skills in:
- MS Visual studio
- C C C#
- User interface frameworks (Win32 GDI WinForms)
- Network communication (TCP/IP WCF)
- Source version control (ex. SVN GIT)
- Unit testing frameworks (ex. CppUnit NUnit)
- Bug tracking systems continuous integration frameworks
- Microsoft Office (Outlook Excel Word etc.)You designed software products in an FDA or other regulated industry.
- You have 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
- You are fluent in French and English. Fluent in German is a big plus
What You'll Bring: You hold a Master's degree or PhD in Software Engineering, Computer Science, or Electrical Engineering You have at least 3 years of experience as a Software Engineer You possess a good understanding and proven experience working under software project methodologies (Waterfall, V-Cycle or Agile) You have strong software skills in: MS Visual studio C++, C, C# User interface frameworks (Win32 GDI, WinForms) Network communication (TCP/IP, WCF) Source version control (ex. SVN, GIT) Unit testing frameworks (ex. CppUnit, NUnit) Bug tracking systems, continuous integration frameworks Microsoft Office (Outlook, Excel, Word, etc.)You designed software products in an FDA or other regulated industry. You have 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 You are fluent in French and English. Fluent in German is a big plus