We seek a senior embedded software professional with strong C++ coding skills for a FDA regulated medical device - equipment for a client in Denver, Colorado.
You will be a skilled object oriented developer who loves to solve complex problems in embedded systems and code in C++. You will have a passion for developing robust, error free software for safety critical medical device - equipment applications. You will be capable of independently defining software requirements, producing a high-level and detailed design from those requirements, and implementing and testing the associated software. Using your coaching and mentoring skills you will provide leadership within the software development team to develop significant and complex software.
Title: Senior Engineer
Location: Denver, Colorado (Denver Tech Center)
Compensation: This is a full-time, direct salaried position. Bonus eligible. Comprehensive benefits package. Relocation assistance is available.
BSEE/CE/CS with 5+ years embedded software design and development. Full life cycle development. Solid C++ coding skills for embedded systems running with or without an RTOS. Skilled in both object oriented design and development, as well as procedural development. Knowledge of software design patterns, test driven development (TDD), unit testing frameworks, and software automation designs and testability. Use of in-circuit emulators, logic analyzers, and oscilloscopes. Knowledge of FDA QSR, IEC, and ISO standards - requirements.
Pluses: MSEE/CE/CS with 7+ years. CppUnit. UML. Technical team leadership. Electronic hardware design.
General: Lead the technical direction of all software development projects from concept to completion. Senior technical reviewer of detailed software design, code, and documentation presented at software design. Translate business and design goals into usable products. Architect and specify hardware and software infrastructure. Responsible for standards and documentation of software development including training of others on the technical staff. . Identify and recommend where new technologies may be incorporated. Perform traditional development activities, such as analysis, design, coding, testing and documentation. Perform testing to identify problems early, perform error and stress scenarios. Participate in design and code reviews. Create test protocols, supervising the testing and test reporting. Contribute to the creation of V&V plans and protocols. Ensure compliance with regulatory requirements particularly FDA Quality System Regulation.
For confidential consideration please send a resume to ... resumes@steinmanrecruiting.com and-or apply at http://www.steinmanrecruiting.com/candidate_center/submit_resume
------------------------------------------------
Technical Recruiting Specialists Since 1982 Steinman Recruiting Associates Littleton, Colorado, USA www.steinmanrecruiting.com
303.798.1058
resumes@steinmanrecruiting.com
Please connect with us through LinkedIn...
www.linkedin.com/in/steinmanrecruiting
Steinman Recruiting Associates specializes in the placement of engineering and technology professionals. With nearing 30 years in the business, you can count on our team-based processes, technical know-how, and ethics. Our commitment is to provide the best service to both our candidates and the companies we serve.
A top producer and member/owner of the Worldwide Recruiting Network with over 350 partner offices in the Americas, United Kingdom, Eastern Europe Australia, India, Japan, China, Hong Kong, Singapore, and S. Korea.
Share this job:
Share this Job
