KMC Operations in
Senior Integration Systems Engineer-Medical Device
KMC Operations in, Merrimack, New Hampshire, us, 03054
Senior Systems Integration Engineer—Electromechanical Medical Device
Merrimack, NH, USA
Job Description Company Information At HiArc, we believe clients don’t need another vendor; they need a strategic partner who gets it. One who listens harder, thinks deeper, and builds smarter—around their needs, products, and goals. HiArc engineers and manufactures complex medical technologies with one goal in mind: creating the perfect fit for our clients. No off-the-shelf thinking. No compromises. Just a tailored, high-performance solution our clients need, the way they need it. That’s why HiArc is the most client‑centered partner in the market. We fuse design, engineering, and manufacturing into a seamless, collaborative process—crafted entirely around our clients. We operate as an extension of our clients’ teams, de‑risking their processes and accelerating their path to market. And the result is a solution you won’t find anywhere else.
Join our team! We hire experts in hardware and software design, robotics, optics, fluidics, chemistry integration, motion and thermal control, risk management, supply chain management, performance testing, advanced manufacturing techniques, finance, human resources, sales, and marketing.
Job Summary At HiARC, Systems Engineers provide leadership for small to mid‑sized cross‑functional program teams to deliver the technical content, performance, intellectual property and quality deliverables for new product development programs. They drive the architecture, vision and design requirements for the product all the time balancing implementation complexity, risks, manufacturability, serviceability and quality. 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. Under close guidance and supervision, apply basic engineering and scientific principles and techniques to assist in the development and establishment of quality assurance programs which provide and maintain the highest quality levels for an assigned project, product, or area.
Responsibilities
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
Required:
Bachelor’s degree in engineering
5 or more years of complex electro‑mechanical instrument systems engineering experience, to include
experience integrating hardware and software
Preferred, but not required:
Medical Device experience (FDA or other regulated design environment)
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.
Benefits
Most locations offer a 9/80 schedule, providing every other Friday off
Competitive compensation & 401(k) program to plan for your future
Robust medical, dental, vision, & disability coverage with qualified wellness discounts
Basic Life Insurance and Additional Life & AD&D Insurances are available
Flexible Vacation & PTO
Generous Employee Referral Program
Voluntary Benefits Available: Longer Term Care, Legal, Identify Theft, Pet Insurance, and more
Voluntary Tricare Supplement available for military retirees
This job description does not list all the duties of the job. You may be asked by your supervisors or managers to perform other duties. The employer has the right to revise this job description at any time. The job description is not an employment contract. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. HiArc, an Elbit America company, is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
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Job Description Company Information At HiArc, we believe clients don’t need another vendor; they need a strategic partner who gets it. One who listens harder, thinks deeper, and builds smarter—around their needs, products, and goals. HiArc engineers and manufactures complex medical technologies with one goal in mind: creating the perfect fit for our clients. No off-the-shelf thinking. No compromises. Just a tailored, high-performance solution our clients need, the way they need it. That’s why HiArc is the most client‑centered partner in the market. We fuse design, engineering, and manufacturing into a seamless, collaborative process—crafted entirely around our clients. We operate as an extension of our clients’ teams, de‑risking their processes and accelerating their path to market. And the result is a solution you won’t find anywhere else.
Join our team! We hire experts in hardware and software design, robotics, optics, fluidics, chemistry integration, motion and thermal control, risk management, supply chain management, performance testing, advanced manufacturing techniques, finance, human resources, sales, and marketing.
Job Summary At HiARC, Systems Engineers provide leadership for small to mid‑sized cross‑functional program teams to deliver the technical content, performance, intellectual property and quality deliverables for new product development programs. They drive the architecture, vision and design requirements for the product all the time balancing implementation complexity, risks, manufacturability, serviceability and quality. 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. Under close guidance and supervision, apply basic engineering and scientific principles and techniques to assist in the development and establishment of quality assurance programs which provide and maintain the highest quality levels for an assigned project, product, or area.
Responsibilities
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
Required:
Bachelor’s degree in engineering
5 or more years of complex electro‑mechanical instrument systems engineering experience, to include
experience integrating hardware and software
Preferred, but not required:
Medical Device experience (FDA or other regulated design environment)
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.
Benefits
Most locations offer a 9/80 schedule, providing every other Friday off
Competitive compensation & 401(k) program to plan for your future
Robust medical, dental, vision, & disability coverage with qualified wellness discounts
Basic Life Insurance and Additional Life & AD&D Insurances are available
Flexible Vacation & PTO
Generous Employee Referral Program
Voluntary Benefits Available: Longer Term Care, Legal, Identify Theft, Pet Insurance, and more
Voluntary Tricare Supplement available for military retirees
This job description does not list all the duties of the job. You may be asked by your supervisors or managers to perform other duties. The employer has the right to revise this job description at any time. The job description is not an employment contract. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. HiArc, an Elbit America company, is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
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