Firmware Engineer - 70 - 80 EUR/hr - Amsterdam - Jan Start

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Firmware Engineer - Amsterdam, Netherlands - January Start - 6 Months - 80% Remote - 70 - 80 EUR/hr

Job Summary & Responsibilities

The Firmware Engineer shall participate in research and product development activities ranging from product concept through transfer to manufacturing. This position will apply knowledge of engineering principles and practices for software development of implantable medical devices and accessories.

Role Requirements
  • Develops embedded and PC-based software, which interact with devices such as an implantable stimulator or wand. Development activities include definition of requirements, design and implementation, and verification and validation.
  • Debugging and analyzing device issues and field returns.
  • Develops software in a regulated environment in accordance with internal operating procedures and external standards and regulations. Conducts cross-functional reviews of the software development at appropriate times in the development cycle.
  • With direction, determines and pursues courses of action necessary to obtain desired results.
  • Applies technical principles, theories and concepts, in addition to developing new development principles and concepts towards the solution of complex technical problems and provides solutions which are innovative and ingenious.
  • Proactively identifies areas of developmental risk and communicates these to the team accordingly.
  • Works in accordance with quality system procedures and actively enforces its objectives.

Skills and Knowledge
  • Knowledge of software design for embedded systems is required.
  • Knowledge of C and an understanding of embedded firmware are also required.
  • Hands-on experience with oscilloscopes, bus analyzers and logic analyzers is desirable.
  • Knowledge of Assembly, C++, C#, and other relevant languages is desirable.
  • It is preferred that this candidate has experience in implantable medical device development.
  • Functional familiarity with the FDA Submission process, ISO Requirements and QSR requirements is also preferred.