Senior Systems Engineer

    Highlights

    Roles & Responsibilities: Perform the activities associated with the systems engineering of one or more products in various stages of the product lifecycle from new product development to post-market surveillance. Creative Problem Solver identify technical risks up front, develop and execute mitigations and provide team direction on how to remove or avoid roadblocks.

    Numbers & Facts

    LocationPlymouth, MN

    Description

    Roles & Responsibilities:
    • Perform the activities associated with the systems engineering of one or more products in various stages of the product lifecycle from new product development to post-market surveillance
    • Understand clinical and user needs and apply them to product realization
    • Capture inputs for requirements from various sources such as user needs, regulatory standards, human factors, quality, manufacturing, service, etc.
    • Use knowledge of technology, process, and/or therapy domains to drive solutions and product design realization from a systems perspective
    • Craft design concepts and research methodologies that best meet current and future customer / business needs for a product or process domain area
    • Create and maintain design history file elements
    • Facilitate an improved understanding of the interrelationship between requirements, risk and reliability
    • Anticipate technical challenges and risk scenarios and prepare, lead, and execute mitigation strategies to ensure optimal results
    • Resolve systems-related technical issues by applying problem-solving tools such as cause-and-effect diagrams, Pareto charts, etc.
    • Propose and drive solutions to technical problems that are ambiguous and diverse in scope
    • Perform impact assessments on the requirements on an ongoing basis for any proposed design / material / process changes or observations from field / service / manufacturing. As needed, propose recommended mitigations with rationale.
    • Influence stakeholders and cross-functional team members within the project
    • Drive adherence to FDA, ISO and IEC design control procedures, regulations and standards
    • Use various software tools and programs to complete the above responsibilities

    Education and Experience:

    • Bachelor's degree or Master's degree and three years or more of relevant experience, with a degree in Electrical, Software, Mechanical, Biomedical, or a related engineering or science discipline
    • Prior experience in medical devices, preferably for intensive care unit (ICU) or kidney care domains
    • Sound knowledge of systems engineering and related areas such as electro-mechanical and software engineering
    • A track record in electro-mechanical system development, preferably in medical devices or other regulated products such as aerospace, automobile, or military
    • Prior experience with internet-connected, software-enabled devices and/or cyber security
    • Working knowledge of system modeling language (SysML or UML) and requirement management tools
    • Knowledge of DOORS and Jama requirements management tools preferred
    • Knowledge of Teamcenter, TrackWise8, JIRA, and ALM preferred
    • Familiar with statistical methods/tools for design and verification, e.g. DOE, sample size
    • Success in working with multi-functional, global teams
    • Excellent interpersonal, communication, and influencing skills
    • Ability to work independently
    • Ability to manage simultaneously several projects and shift priority according to needs
    • Demonstrated strong analytical and problem-solving skills
    • Ability to solve problems, develop solutions, and make recommendations in collaboration with project leaders
    • Creative Problem Solver identify technical risks up front, develop and execute mitigations and provide team direction on how to remove or avoid roadblocks
    • Ability to deliver results according to the plan

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