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    R&D Engineer - Brooklyn, United States - Synchron LLC

    Synchron LLC
    Synchron LLC Brooklyn, United States

    4 weeks ago

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    Description

    **R&D Engineer (Therapy Delivery / Leads)**

    at Synchron Brooklyn, New York, United States **About Synchron**

    Synchron is developing a platform of brain interface technology that transmits data in and out of the brain via devices implanted inside cerebral blood vessels using minimally invasive endovascular procedures (Neuro-Intervention).

    As a leader in brain-to-machine communication, Synchron is poised to create a significant impact in its industry and to meaningfully impact many peoples lives. Whilst the companys technology is maturing fast (4 clinical trial participants have already benefited from the first-generation device), there is an opportunity to help shape the companys direction and to work in a dynamic, multi-disciplinary and growing team.

    We are a lean, fast-paced, passionate team pushing the boundaries of what is possible in the neurotech space to dramatically improve the quality of life of millions of people globally, and we want you to join us.

    **Position description: R&D Engineer Therapy Delivery / Leads**

    The successful candidate will join the hardware team and be responsible for the design and development of novel system components to produce a commercial-ready Brain-Computer Interface (BCI) device.

    The system comprises of active implantable components and non-implantable elements that facilitate signal communication to everyday devices. This role focuses on therapy delivery type leads that feature a unique interface to capture brain signals within the venous system.

    As a team member, this individual will contribute as part of a cross functional team to FDA submissions. This role requires experience working in a regulated industry, such as chronically implanted active implanted medical devices.

    This team member will work collaboratively with internal and external resources to drive on-schedule device builds. Experience in the planning and execution of design verification for complex medical devices is beneficial, in addition to experience contribution to Risk Management documentation. Competency in 3D modelling (Solidworks) is a bonus.

    **Knowledge & Key Skills:**

    5+ years of experience in a highly regulated industry.

    BS in Mechanical engineering, Biomedical Engineering, or related technical field.

    Experience in the design and manufacturing of implanted medical devices that are commercial-ready.

    Experience developing test methods, protocols, and reports.

    Experience with validating test methods and qualifying test equipment.

    Results-oriented with a combination of mental flexibility, creativity, analytical ability, and sound judgment.

    Personal drive, adaptability, individual accountability, and a strong bias for action.

    Excellent organizational, communication, and collaboration skills.

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