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As a Technical Recruiter at Neuralink, you'll enhance the talent acquisition strategy by sourcing and managing candidates for technical roles, collaborating with hiring managers, attending candidate debriefs, and continuously improving recruiting initiatives to build a strong network of exceptional talent.
As a Quality Systems Specialist, you will resolve problems through non-conformance reports (NCRs) and corrective actions (CAPAs). You'll manage document control, oversee regulatory compliance, analyze defects, and collaborate with R&D, manufacturing, and product teams to enhance quality processes and systems.
The Design Assurance Engineer will ensure compliance with regulatory standards in the development of software for medical devices. Responsibilities include risk management, facilitating design transfer to manufacturing, participating in design reviews, and generating risk management documentation. The role involves collaboration with cross-functional teams and requires strong analytical and quality assurance skills.
The Site Reliability Engineer will collaborate with cross-functional teams to enhance system operations, drive best practices in software engineering, and build infrastructure for Brain-Computer Interface tasks. Responsibilities include deploying hardware, managing cloud architecture, monitoring operational efficiency, and ensuring systems are secure and reliable.
The EPC Engineer is responsible for ensuring construction projects meet technical requirements and specifications. Duties include inspections, contractor scheduling, responding to RFIs, and approving contractor invoices. They participate in meetings to address technical questions, conduct constructability reviews, and generate reports and protocols for quality control, ensuring alignment with design intent during construction.
The Quality Assurance Specialist ensures compliance with regulatory standards in the medical device sector by conducting inspections, audits, and training. Responsibilities include maintaining study protocols, reviewing quality assurance documentation, and preparing compliance reports. This role also involves liaising with FDA during inspections and ensuring that quality control processes meet established standards.
The OR Specialist will be responsible for surgical case coverage in the Operating Room during implantation of the implant as well as process improvement projects. Duties include data collection, SOP writing, product support, and collaboration with surgeons and staff.
The Senior Digital IC Verification Engineer will lead functional verification for neural recording and stimulation SoCs, focusing on low-power processors and digital signal processing. Responsibilities include developing automation flows, building test benches, debugging, and ensuring code quality through coverage and regression setups.
The Senior Embedded Software Engineer will work on developing high-performance, safety-critical embedded systems for brain-computer interfaces, engaging with cross-disciplinary teams, and solving complex problems in embedded technology. The role emphasizes delivering reliable solutions and collaborating with engineers and designers.
As a Systems & Process Engineer, you will gather requirements and develop compliant processes, enhance efficiency, and drive continuous improvement using quantitative metrics. Responsibilities include process optimization in various areas such as manufacturing and audits, and collaborating on deviations and audit findings.
The Digital IC Design Engineer will focus on the design and implementation of low-power digital signal processors and hardware accelerators. Responsibilities include micro-architecture design, RTL implementation, optimizing hardware/software interfaces, and collaborating on silicon tests with verification engineers.
As a Software Engineer in Robotics, you will write and test software for surgical robots, ensuring functionality beyond simulation. You will work with high-precision mechanical systems and integrate devices while having a collaborative and communicative role within a meritocratic environment.
Design and manage the development of neuroprosthetic devices, focusing on minimizing tissue reaction and maximizing signal-to-noise ratio. Collaborate with cross-disciplinary teams on board design, chip integration, and manufacturing processes. Oversee product verification and validation phases and work on embedded systems for high-reliability applications.
The Technical Recruiter will engage in sourcing, interviewing, and managing talent pipelines across various technical roles. They will collaborate closely with hiring teams to improve recruitment strategies and build strong relationships with candidates and hiring managers. The role requires proficiency in evaluating candidates and utilizing recruiting tools effectively.
As a Firmware Engineer, you will develop and optimize embedded software for robotic surgery applications, refine legacy software, perform rigorous testing, write drivers, and collaborate on hardware specifications and software enhancements.
As a Senior Embedded Software Engineer, you will be part of a team working on high-performance, safety-critical embedded systems for brain-computer interfaces. Your role involves problem-solving, delivering reliable solutions, and collaborating with cross-disciplinary teams on firmware development that impacts product capabilities.
The Digital IC Design Engineer will be responsible for creating micro-architecture and RTL implementation of digital systems focused on low-power DSPs and hardware accelerators for brain-computer interfaces. Responsibilities include design optimization, collaboration on silicon tests, and balancing power/performance while working with firmware engineers.
You will be responsible for writing software to ensure it operates on a surgical robot. The role emphasizes hands-on experience with robotics and high-reliability systems, focusing on high-precision mechanical motions. Strong coding skills in Linux and system languages are essential for this position.
The Quality Systems Specialist will collaborate across teams to address quality issues, manage document control, oversee CAPAs and NCRs, analyze trends to improve processes, and ensure compliance with regulatory standards in the medical device industry.