System Engineer - Electrical Summer 2025 start date
System Engineer - Electrical Summer 2025 start date
Posted on :
17-03-2025
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1 Vacancy
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Job Description
About us
Neocis is an established startup revolutionizing dentistry with Yomi the first and only FDA cleared robot for assisted dental surgery. The company collaborates closely with leading clinicians to develop innovative technologies that help advance patient care and improve quality of life. Based in Miami Florida. Neocis is venturebacked with funding from several prominent investors.
Whats in it for you
- Youll thrive in our innovative and collaborative environment
- Make an immediate impact on lifechanging technology
- Avoid silos and not my job mentality in our smaller fast paced startup environment
- We offer sabbatical parental leave and unlimited PTO policies
- Generous 401K plan with 4 company match
- Comprehensive benefits package that includes medical dental and vision.
Start date:This position will start around Summer 2025
The Role: As a key member of our Hardware team youll be contributing to the design and development of our current and next generation robotics system. With focus on the electrical side of our platform the Systems Engineer will be responsible for defining and improving system architecture of our robotics platform.
What youll do:
- Lead projects for definition and improvements of system architecture with focus on electrical components
- Develop modeling simulation and estimation to understand the impact of electrical components on system performance (signal quality communication protocols latency sensor specs power delivery emission reliability)
- Develop system architectures quickly identifying and resolving bottlenecks and conflicts across subsystems and components from different domains
- Development of initial prototypes and R&D demonstrator towards improved performances and/or reliability of electrical and electronics components.
- Perform risk analysis to help guide design of safe medical devices
- Generate highquality technical documentation for both establishment of new solutions and continuous development of existing designs
- Define and iterate subsystem specifications and requirements
- Design and development of testing processes with specific focus on relevant and meaningful metrics to harmonize equipment verification and desired performance
- Effectively work with crossfunctional teams including mechanical software and electrical engineers as well as clinical project management product development and marketing staff
- Support improve and educate regarding Verification and Validation activities as well as advanced troubleshooting for systems field or manufacturing roadblocks
- Followup with lifecycle teams (quality manufacturing operation) to ensure newly introduced products or processes maintain a high standard of reliability and performance
- Directly contribute to product development by proposing novel solutions and approaches for enhanced system performance and new applications
What youll bring:
- BS degree in Electrical Engineering required plus a MS degree with focus on Robotics
- Strong understanding of robotic principle (kinematic and dynamic modeling control theory)
- Proficient in Schematic capture PCB layout PCBs bringup and prototyping DfM and DfA
- Experience with mixedsignal electronic design for precise sensing preferred
- Proficient in use of and maintaining laboratory equipment (power supply oscilloscope multimeter solder station signal generator)
- Demonstrated knowledge of analog and/or digital design
- Strong robotics programming (e.g. Python C C) skills and experience with robotic packages
- Problemsolving skills with ability to abstract and generalize
- Experience in documenting and testing electromechanical systems
- Excellent communication teamwork interpersonal skills with the ability to selfdirect required
- Experience with datacollection via basic interfaces (e.g. Arduino DAQ) and data postprocessing and statistics (e.g. Matlab Python Minitab) preferred
- Experience with medical devices preferred
- Experience with the following regulations preferred:
- FDA 21 CFR Part 820 FDA Quality System Regulation
- IEC 606011 Safety standard for electromedical devices
- ISO 13485 Medical Devices Quality Management Systems Requirements for Regulatory Purposes
What else
This is a fulltime position. This position occasionally requires long hours and weekend work.
This position requires up to 10 travel. Frequently travel is outside the local area and overnight.
This job operates in a professional office/manufacturing/clinical environment.The main location of this role is in a medical devices manufacturing facility and requires:
- The regular use of CMMs and machining equipment and occasional use of CBCT scanners
- Prolonged periods working on a computer
- Ability to lift/push/carry items up to 50 pounds
- Frequent exposure to loud/moderate noise
Please note this job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. Duties responsibilities and activities may change at any time with or without notice.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Employment Type
Temp
Key Skills
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