Careers at KMC Systems
KMC Systems is a leading contract designer and manufacturer of medical devices and instrumentation for OEM’s in the areas of life science diagnostics, therapeutics, and biomedical products.
KMC is an ISO 13485 certified and FDA registered firm with expertise in all aspects of medical instrumentation product development, design, manufacturing, and field support. A complete suite of services are available across the Total Product Life Cycle through our KMC360® program.
KMC Systems was recognized as one of the best companies to work for in New Hampshire by Business NH Magazine. Add in our employee-friendly corporate culture and great southern New Hampshire lifestyle, and you’ll see why joining ESA-KMC Systems could be the best move of your career. Don't miss the opportunity to work for a great company. Apply now.
KMC Systems, Inc. is a wholly owned subsidiary of Elbit Systems of America. Elbit Systems of America is proud to be an Equal Opportunity Employer: Minorities, Females, Protected Veterans and Individuals with Disabilities.
Are you a strong team leader who can manage software quality assurance resources and activities with a focus on zero defect deliverables? In this role, you would be responsible for the people, processes, and tools to ensure the timely and cost‑effective design and implementation of software verification and validation plans/procedures to ensure our software deliverables are compliant with customer specifications and regulatory requirements. If you have demonstrated collaboration skills and track record of high quality performance, click here to learn more and apply online.
Are you an experienced business development professional in the medical device design and manufacturing space looking for a real opportunity? Can you identify, develop and nurture relationships to close business for a medical device design and manufacturing service provider? Click here to learn more and apply online for Business Development Manager
Design, implement, and deliver reliable, high quality, robust embedded and desktop software for complex medical instruments meeting regulatory standards. A great opportunity for a SWE with C/C++ and design experience of software for hardware instruments/devices that include motion control interfaces. Click here to learn more and apply online for Principal or Senior Software Engineer.
In this entry-level opportunity, you will join a team of expert software engineers and participate in the development of software design and code as well as testing and analysis of high-quality embedded and desktop software for complex medical instruments. You will have the opportunity to work on a variety of projects that may utilize C/C++, Java, or C#. Experience with software for hardware instruments/devices is a plus. Internship or lab experience is an advantage. Click here to learn more about the Software Engineer opportunity.
Can you lead our systems engineering team providing technical, process and people leadership? Are you skilled at working with program management and other engineering disciplines to define and execute a systems engineering department and organizational development strategies to yield a “best in class” team? Click here to learn more and apply online for the Systems Engineering Manager position.
Can you provide technical leadership over complex, major design, development and research projects, develop design and product performance specification requirements and evaluate and select optimum design alternatives as a senior mechanical engineer? Click here to learn more and apply online for Senior Mechanical Engineer - Fluidics.
Do you have experience with architect and design of software for complex medical devices? Do you have the ability to work collaboratively with a team to develop cost effective yet efficient software programs? If you're looking to grow your career while developing and designing complex software coding, click here to learn more and apply online for Software Architect.
Assure that product development engineering activities are completed to meet applicable regulatory requirements, published standards, the requirements of the Quality Management System and the objectives of the assigned contract. Positively impact trial designs, ensure customer’s regulatory submission success, and keep products on the market. Serve as a resource to the Engineering staff during product development and provide technical direction with respect to EMC, EMI, Safety, and Environmental design issues. Click here to learn more and apply online for Regulatory Compliance Engineer.