Senior Systems Engineer-Medical Device Engineering - Merrimack, NH at Geebo

Senior Systems Engineer-Medical Device

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 The Systems Engineer must understand and capture the user needs into system requirements.
The System Engineer helps to ensure that the quality targets are satisfied and retires technical risks as they arise on the program.
The Systems Engineer maintains close interaction with customers to understand and enhance the ability to deliver customer satisfaction through higher product quality.
Job Description Lead effort to create system level concepts for new project proposals.
Review and critique concepts created by others Ability to prepare Systems Engineering cost and schedule estimates on major design development efforts.
Provide technical presentation support and consultation to marketing for proposals and during development.
Plan and lead experiments to evaluate operating characteristics of products or processes.
Translate experimental results into design criteria.
Support System Integration, Verification and Validation by defining, specifying and supervising testing, analysis and integration activities.
Ensure reports are prepared to document the results of such activities.
Support the design review and phase gate process to ensure that engineering deliverables are at the appropriate level to meet FDA/ISO requirements & standards.
Accountable to oversee the development of requirements for different disciplines such as Software, Electrical, Mechanical, Electro-optics and others.
Qualifications Bachelor's Degree in Engineering 5 years of complex electro-mechanical instrument systems engineering experience Hardware / software integration experience.
Must be available for daily onsite presence Preferred Requirements:
Master's degree in Engineering.
Medical Device experience Extensive development experience in at least one or more of the following engineering disciplines is required:
software, mechanical, electrical, optics, fluidics and should possess knowledge of advanced theories, concepts, principles, and processes.
Ability to provide technical leadership as required during the investigation of complex medical instrumentation products.
Accountable to oversee the development of requirements for different disciplines such as Software, Electrical, Mechanical, Electro-optics and others.
#LI-SW1 #LI-Onsite Additional Information All your information will be kept confidential according to EEO guidelines.
Recommended Skills Consulting Customer Satisfaction Electromechanics Experimentation Fluidics Instrumentation Estimated Salary: $20 to $28 per hour based on qualifications.

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