Medical Device Systems Engineer

Associates Systems

  • Parsippany, New Jersey
  • 30+ days ago

    Highlights

    Under auspices of the Program Manager, leads efforts to allocate system functionality among electronic/software/mechanical subsystems, make hardware/software/mechanical trade-off decisions, cost/time/performance trade-off and safety decisions necessary to meet the product’s clinical performance, reliability, manufacturability/serviceability, regulatory and business objectives. Working knowledge and experience with low level analog signal acquisition, digital/microprocessor systems design, power supplies, embedded real time software development, digital signal processing, real time operating systems, Analog/digital control systems, displays, batteries, data storage and wireless communications systems.

    Numbers & Facts

    LocationParsippany, New Jersey

    Description

    ob Summary:

    Highly experienced, cross-functionally skilled technical leader (electrical/software/mechanical) responsible for the system level architecture/design, implementation and verification of complex systems (e.g. defibrillators, patient monitors, ventilators) in a matrix setting.

    Essential Functions:

    • Works with Project/Program management to establish and refine system level requirements for assigned new and enhanced products.

    • Leads development team in translating system level requirements into product architecture and system level design including partitioning functionality into sub-systems, creating specifications for each sub-system and documenting the interface requirements among the sub-system.

    • Ensures that new product architecture meets system level requirements, is appropriately featured, robust and adaptable enough to support product lifecycle plans and objectives.

    • Establishes performance, interface, safety, and cost specifications for each sub- system within the selected architecture in consultation with the functional design leaders. Contributes significantly to the system level risk management activities associated with assigned programs.

    • Under auspices of the Program Manager, leads efforts to allocate system functionality among electronic/software/mechanical subsystems, make hardware/software/mechanical trade-off decisions, cost/time/performance trade-off and safety decisions necessary to meet the product’s clinical performance, reliability, manufacturability/serviceability, regulatory and business objectives.

    • Leads efforts during the product implementation phase to develop and refine the system level design, identify and resolve sub-system performance and interface issues, and resolve cross

    • functional design issues that have system level impacts.
    • Leads/oversees team efforts during the subsystem integration and verification testing phases to ensure that critical sub-systems meet their individual performance, interface and system integration goals and to ensure that the fully integrated system robustly meets its performance, safety and cost requirements.

    • Responsible for documenting the system level design, operating principles and sub-system interface specifications for his/her assigned new and existing products.

    • Researches and documents the relationships between clinical requirements, architectural decisions, performance requirements and product evolution plans.

    • Provides advice and consultation to engineering teams regarding system engineering principles and system level requirements of  

    • products. Actively participates in decision making processes that involve changes to the system level design of existing products.

    Skills Requirements:

    • Extensive knowledge and experience in the system level design and development of multi• processor based medical instruments containing biomedical signal acquisition and processing electronics and embedded software systems.

    • Demonstrated ability to translate high level product requirements into system and sub- system level specifications and designs.

    • Demonstrated success leading engineering teams in the architecture, system level design, integration and verification of portable, battery operated, multi-processor based measuring and/or patient treatment systems.

    • Working knowledge and experience with low level analog signal acquisition, digital/microprocessor systems design, power supplies, embedded real time software development, digital signal processing, real time operating systems, Analog/digital control systems, displays, batteries, data storage and wireless communications systems.

    • Working knowledge of mechanical engineering issues and processes associated with electronics packaging, small moving mechanisms, molding, and machining processes.

    • Ability to independently analyze and evaluate electronic circuitry, software and mechanical designs using drawings, schematics, source code, technical education, and experience.

    • Thorough understanding of the product development and engineering project management processes.

    • Experience with and sensitivity to human factors issues associated with the use of medical devices.

    • Knowledge and experience developing products under FDA and European Community medical device regulations and standards.

    • Excellent verbal and written communications skills. Demonstrated success in technical decision making and people management/leadership in a matrix environment.

    • Ability to handle confidential information with discretion and skill.

    • Business acumen.

    Required/Preferred Education and Experience:

    • Advanced degree in Engineering including training and experience in systems, electronics, software and mechanical engineering.

    • 10+ years' experience developing electronic hardware and embedded software systems/subsystems for complex, real time measuring instruments.

    • 7+ years' experience as a Systems Engineer, leading the architectural design and systems engineering of complex, real time medical measuring instruments.

    • Knowledge of fluid mechanics and/or past experience with ventilators/aspirators is required.

    • Project management experience and training.

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