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Lead Software Engineering Manager

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Location: Los Angeles, CA

Purpose of Role:
• Design, develop, document and maintain the software architecture in collaboration with the system engineering team. • Provide technical leadership and define, develop, and evolve software using the latest software development technologies and infrastructure. • Translate requirements into design, and deliver to required timelines and quality standards. • Determine and create detailed design for each assigned code modules. • Develop automated test wrappers for each code module. • Implement code modules in C, C++, C# and Java depending on requirements and fully document code modules and integrate code modules with other system components. • Construct overall test strategy and perform unit, functional and integration and related software V&V testing. Publish protocols and test reports. • Maintain software bug tracking system. Write and publish software release packages which include known bugs. Create system error codes and track. • Publish a full suite of documentation such as software architecture, software design description, software development plan, software requirement specifications, traceability and bug tracking, software verification and validation plans Requirements of the Position: • A minimum Bachelor’s degree in Computer Science or similar degree with commensurate experience required. A Master’s degree is preferred. • 8+ years of professional C/C++, C# or Java experience required with demonstrated deliverables including code, documentation and team leadership. • Multi-threaded programming experience required. • Experience in all phases of the development lifecycle including design, implementation, debug, verification and validation required, • Experience with development of medical instrumentation that are in compliance with US FDA regulations preferred. • Experience preferred in at least three of the following areas: Image Processing, Graphical User Interfaces, OpenGL, Network programming with TCP/IP sockets, Robotics, PID Control Systems and cross-platform development tools (such as QT, Boost). • As an individual researcher this position requires application of company safety and quality policies and procedures, assisting as a staff consultant on technical issues and the identification and protection of intellectual property related to the treatment device. Support of regulatory submission, QA and ISO registration activities is also required Qualified candidates please reply to: Cindy Johnson cjohnson@chozeninc.com tel: 925-577-8135


Contact Information:

E-mail: cjohnson@chozeninc.com

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Chozen, Inc. 21001 San Ramon Valley Blvd., Suite A4-147, San Ramon, CA 94583  T: 925.242.1010 F: 925.886.8600