Sr. Software Engineer - Medical Devices - (REF2471W)

Company Description

KMC Systems, an Elbit Systems of America company, offers an ecosystem of engineering and innovation to develop the most advanced clinical and operational solutions for leading medical device customers across a diverse range of market segments. KMC was established in Merrimack, NH, in 1980, conveying almost half a century of innovation, R&D of next generation devices, and the agility to evolve to meet changing market dynamics. This has kept KMC at the forefront of technological advancements and as the premier choice for leading global medical device and healthcare companies. KMC is a full-suite provider with services in: Engineering Design, Manufacturing, Product Ideation, Product Lifecycle Management, and Sustaining Engineering. We are looking for extraordinary people to join #OneTeamOneMission to create and deliver innovative solutions that protect and save lives.

Job Description

Are you a strong Sr. Software Engineer who collaborates with other high quality, dedicated engineering professionals? Looking for purpose? You would have the opportunity to develop cutting edge Medical Device products that are used every day to improve people’s health and well-being. 

This opportunity requires a driven engineer willing and able to tackle complex and challenging technical issues using their expertise and ingenuity. You will enjoy a culture that values hard work, creativity, and getting the job done; will work side by side with other dedicated engineers across a range of disciplines; and will know that the products that they take to market will ultimately make real improvements in people’s lives.                

Don’t let this opportunity to make a difference pass you by.  Check it out and Apply!

We spend our days working on exciting and meaningful innovative solutions that protect and save lives.  From providing solutions for our warfighters and commercial pilots, to providing lifesaving medical instrumentation and homeland security technologies, the employees understand the value of their work and why we do what we do each and every day.  We are looking for extraordinary people to join us in making a difference in the lives of others.

Job Description

Responsibilities

·       Design, implement, and deliver reliable, high quality, robust embedded and desktop software targeted to complex medical instruments meeting regulatory standards

·       Create, maintain, and review software project documents including software development plans, software configuration plans, and detailed software design documents

·       Participate in software project risk analysis and hazard analysis

·       Drive software requirements with other members of the software team as appropriate (team lead, architect, etc.) and proactively work to integrate with system requirements

·       Participate in Software Change Control Boards, and participate in the investigation and resolution of software defects

·       Utilize software engineering best practices (e.g., unit testing, integration testing, static analysis, code reviews, design reviews, Doxygen documentation)

·       Develop software within Continuous Improvement development process

·       Improve Continuous Improvement process (recommend process improvements, software tools, and helper scripts)

Work cooperatively within the software group as well as across disciplines such as systems, electrical, optical and mechanical to deliver projects on-time and on budget

Qualifications

Required:   

• Bachelor’s degree in Computer Science, Electrical Engineering, Mathematics, or related discipline (Master’s degree preferred)
• 5 or more years of relevant experience developing software for complex instrument or devices that include motion control and fluidics
• Demonstrated experience in object-oriented design methodology and programming languages, primarily C# and C++
• Understanding of revision control systems and issue tracking systems
• Ability to work independently or in a team environment
• Strong oral and written communication skills
• Able to work on multiple projects simultaneously (Good organizational and multi-tasking skills)
• Demonstrated experience in software development lifecycle (Agile, Spiral), object-oriented design methodology and programming languages including JAVA ,C/C++, and C#
• Design experience of software for hardware instruments / devices that include motion control interfaces
• Experience with medical device regulatory standards such as 21 CFR Part 820, IEC 62304 and ISO 13485 including experience with system risk / hazard analysis or other highly regulated industry.
• Experience with software configuration tools for source code control (CVS, SVN, PerForce), issue tracking