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    R&D Engineer II - Minneapolis, United States - Philips Iberica SAU

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    Job Title R&D Engineer II – Advanced Development (Plymouth, MN) Job Description

    R&D Engineer II – Advanced Development (Plymouth, MN)

    As part of the Advanced Development team, you have the opportunity to work on new technology and product development alongside other engineers and cross-functional partners to make a significant impact in the medical field.


    Your role:


    Work closely with the design engineers to implement novel procedural improvements by demonstrating a strong knowledge of clinical workflow, device usage and imaging analysis.

    Participate in project team development activities by designing and executing exploratory bench, animal and cadaver studies to test vascular devices and support the design and development phase.

    Use hands-on, iterative prototyping skills to experiment and explore new product ideas on the bench and in animal models
    Create and explore ideas for diseased model/clinically relevant test beds to evaluate products and technologies for peripheral vascular diagnostics and therapy alongside other experienced engineers and scientists to develop new, innovative medical products

    Work with physicians, regulatory, clinical, marketing, and strategy partners to develop concepts and technologies to feed a platform for product development.

    Role is based in Plymouth, MN. Some travel will be required for project work, up to 25%.
    You're


    the right fit if:


    You have at least 2 years of experience in the medical device product development industry, having supported design and development cycles, and can be creative and design a variety of solutions, working with other engineers and technicians.

    You have a Bachelor of Science in Engineering discipline (Mechanical, Materials Science, Biomechanical, Bioengineering, Biomedical) required.
    You have experience supporting preclinical animal and cadaver evaluations and the desire to lead them.
    You are detail oriented and able to provide thorough reviews and authorship of preclinical protocols and reports.
    Your skills include the desire to be hands-on to translate clinical workflow into appropriate bench and animal models to test device designs
    You have working knowledge of interventional medical procedures and disease states applicable to peripheral and coronary vascular system, preferred.
    About Philips
    We are a health technology company.

    We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve.

    Do the work of your life to help improve the lives of others.
    Learn more about

    our business .
    Discover

    our rich and exciting history.
    Learn more about

    our purpose.
    Read more about

    our employee benefits .

    If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply.

    You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion

    here .
    Additional Information
    US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
    Company relocation benefits

    will not

    be provided for this position. For this position, you must reside in

    or

    within commuting distance to Plymouth, MN

    .
    #LI-PH1

    This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates.

    Interested candidates are encouraged to apply as soon as possible to ensure consideration.
    Philips is an

    Equal Employment and Opportunity

    Employer/Disabled/Veteran

    and maintains a drug-free workplace.

    #J-18808-Ljbffr

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