Medical Device Software Development Lead || Oberkochen, Germany || Contract

Beschreibung

We are hiring for Medical Device Software Development Lead || Oberkochen, Germany || Contract


My name is Aswini Rajesh and I am from Adroit People Limited. Please find the details of the opportunity below. If interested in being considered or to learn more, please send me an updated copy of your resume in Word format and furnish the below details and let me know the best time to reach you so that we can discuss regarding this position further.

For more job opportunity add me to you LinkedIn Aswini Rajesh Ponasanapalli.

Role: Medical Device Software Development Lead
Hiring Mode: Contract
Location: Oberkochen, Germany

Job Description:
Development
o Working experience in embedded software development using C and C++ .
o Object-oriented programming knowledge
Process
o Working experience in ISO 13485 QA process and regulatory requirements (like FDA’s PMA, 510k, Cyber security etc.)
o Working experience in Class III Medical device Software development process
Domain Skills: Class III Medical Device
• Overall 15 + years of experience in Medical device SW development lifecycle
• Experience in Risk / Hazard analysis
• Knowledge in Premarket Approval (PMA) process for class III medical devices
• Understand customer requirements and conceptualize solutions that address key needs. Ability to create requirements into implementable software design.
• In-depth knowledge of current technological trends, developments and best practices in the area of information security, wireless network architecture, Cloud and mobile development.

Technical Skills: C and C++
• 10 + years of experience in embedded software development using C and C++
• Knowledge of object-oriented analysis, object-oriented design, and object-oriented programming
• Should have experience is using multiple development tools like TFS, ReSharper, NUnit, NCover, Memory Profilers etc.
• Work with the development team in software design and reviews. In-depth knowledge of designing applications and design tools.

Process Skills: ISO 13485
• Working experience in ISO 13485 QA process and regulatory requirements (like FDA’s PMA, 510k, Cyber security etc.)
• Working experience in Class III Medical device Software development process
Qualification:
A master’s degree in computer science, electrical engineering, industrial engineering or a comparable qualification

Thanks,
Aswini Rajesh
Email: