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Chemist
Neuralink · Austin, Texas, United States
Pay
$71k–119k
Setting
On-site
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Chemist
Austin, Texas, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Biocompatibility Team is responsible for executing a wide range of assays, performing method validations, finalizing reports, and supporting R&D activities. We are a dedicated group of highly skilled professionals committed to ensuring the accuracy, reliability, and regulatory compliance of test methods used in quality control. With deep expertise in analytical techniques, including chemical characterization, microbiological testing, and biocompatibility evaluations, as well as manufacturing processes such as cleaning, sterilization, and passivation, this team plays a critical role in maintaining the highest standards of product quality and patient safety.
Job Description and Responsibilities:
The Chemist will collaborate with cross-functional teams across Neuralink to analyze the chemical and biological characteristics of manufacturing processes and finished devices. This role involves various levels of product testing during R&D and product release to generate data required for regulatory approvals. The data produced will help confirm patient safety in accordance with applicable global regulations, regulatory guidelines, and voluntary consensus standards.
Daily responsibilities include drafting internal procedures and test protocols, sample preparation, laboratory testing, method development, inventory management, and other general laboratory tasks. The primary goal of the Chemist is to support medical device chemical and biological characterization to ensure patient safety and facilitate regulatory approval. Additional responsibilities include:
Preparing test samples and controls for analysis
Performing chromatographic and mass spectrometric analysis using instruments such as LC-MS, GC-MS, and ICP-MS
Conducting routine and non-routine testing of materials and products to ensure compliance with quality standards and regulatory requirements, including performing calibration checks and maintaining proper documentation
Delivering test results related to device characteristics to support manufacturing changes and risk assessments
Preparing laboratory reports that comply with applicable medical device evaluation standards and FDA/ISO guidance documents within a risk-based framework
Collaborating with cross-functional teams to support multiple projects, ensuring timely completion of laboratory deliverables to meet project timelines
Analyzing test results to determine whether data meets internal and external requirements; utilizing problem-solving skills and technical expertise to troubleshoot unexpected outcomes
Participating in continuous improvement initiatives to increase laboratory efficiency, reduce turnaround times, and enhance data quality
Required Qualifications:
Bachelor of Science in Chemistry, Biochemistry, or a related field
1-2 years of experience in an analytical laboratory
Strong knowledge of basic laboratory operations, including weighing, sample handling, and preparation of volumetric solutions
Ability to perform routine analytical chemistry calculations (for example, dilutions, concentrations, and result calculations)
Basic understanding of laboratory safety and proper use of engineering controls (for example, fume hoods and biological safety cabinets)
Demonstrated ability to develop and optimize analytical methods for efficiency and compliance
Strong problem-solving mindset
Excellent written and oral communication skills
Preferred Qualifications:
Master’s degree in Chemistry, Biochemistry, or a related field
Familiarity with Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP)
Hands-on experience with LC-MS, GC-MS, and ICP-MS
Familiarity with chromatography data systems
Experience with statistical analysis
Experience troubleshooting analytical instrumentation
Experience performing bioanalytical procedures and cell-based assays
Experience with method validation and transfer
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$71,000 - $119,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.
Field Clinical Engineer
Neuralink · Austin, Texas, United States
Pay
$89k–250k
Setting
On-site
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Field Clinical Engineer
Austin, Texas, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what’s possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink’s BCI technology for use in people!
Job Description and Responsibilities:
As a Field Clinical Engineer, you will be on the front lines of Neuralink’s clinical programs, working directly with participants, clinicians, and internal teams to translate cutting-edge neurotechnology into meaningful functional outcomes. This role is ideal for individuals with a background in PM&R, occupational therapy, or physical therapy who also have experience in medical devices and thrive in dynamic clinical environments.
You will play a critical role in bridging clinical care, engineering, and research by supporting device use, optimizing participant performance, and ensuring high-quality data collection in both clinical and home settings.
This role requires someone who is hands-on, clinically grounded, technically curious, and able to adapt quickly. You should be comfortable working with participants with significant neurological impairments and motivated by improving independence and quality of life.
In this role, you will:
Work directly with study participants to support device use, training, and optimization during clinical sessions and at home
Apply principles of rehabilitation (PM&R, OT, PT) to maximize participant outcomes and functional performance with the system
Collaborate closely with surgeons, investigators, and site staff to ensure seamless clinical execution across all phases of the study
Serve as the primary interface between participants and the technology, troubleshooting issues in real time and escalating when needed
Support surgical and post-operative workflows, including intraoperative and early post-implant sessions where applicable
Ensure high-quality, protocol-compliant data collection by aligning participant activities with study endpoints and data capture requirements
Partner with clinical, engineering, and data teams to translate real-world use into actionable insights for product and algorithm development
Identify trends in participant performance, usability challenges, and safety signals, and communicate clearly to cross-functional teams
Contribute to development and refinement of training protocols, user workflows, and clinical best practices
Support site onboarding, training, and ongoing engagement to ensure consistency and scalability across clinical sites
Assist in preparation for regulatory inspections and ensure activities are conducted in compliance with GCP, protocol requirements, and internal procedures
Travel to clinical sites as needed to support study execution and participant care
The ideal candidate:
Has a clinical background in PM&R, occupational therapy, or physical therapy, with hands-on experience working with neurological populations (e.g., SCI, ALS, stroke)
Has experience working with medical devices in a clinical or field-based role
Is highly adaptable, proactive, and comfortable operating in a fast-paced, evolving environment
Is technically curious and able to engage with engineers to troubleshoot and improve system performance
Communicates clearly and builds trust with participants, clinicians, and cross-functional teams
Is detail-oriented and understands the importance of protocol adherence and data integrity in clinical research
Required Qualifications:
Clinical training and hands-on experience in PM&R, occupational therapy, or physical therapy, with a focus on neurological populations (e.g., SCI, ALS, stroke)
3+ years of experience in a clinical, field-based, or medical device–adjacent role (rehab, neuromodulation, assistive technology, or similar)
Demonstrated experience working directly with patients and clinicians in dynamic care environments
Strong problem-solving skills with the ability to troubleshoot clinical and technical issues in real time
Ability to interpret participant performance, functional outcomes, and device behavior to inform next steps
Comfort working with technology, including basic data review and interaction with software-driven systems (no need to be a coder, but not afraid of one either)
Working knowledge of clinical research principles, including protocol adherence, endpoint-driven activities, and data quality expectations
Familiarity with Good Clinical Practice (GCP) and general clinical study conduct
Ability to collaborate effectively across clinical, engineering, and operations teams
Strong communication skills, with the ability to engage both participants and highly technical teams
High attention to detail, with the ability to manage multiple participants, sites, and priorities simultaneously
Willingness to travel frequently to support clinical sites and participants
Preferred Qualifications:
Degree or formal training in bioengineering, biomedical engineering, or a related field, with exposure to neurotechnology or implantable systems
Experience working with neuromodulation, brain-computer interfaces, or other neurorehabilitation technologies
Prior experience in a clinical field engineer, clinical specialist, or applications role within a medical device company
Experience supporting surgical procedures, intraoperative environments, or early post-implant programming and troubleshooting
Familiarity with signal-based systems (e.g., neural data, EMG, EEG) and comfort interpreting system performance in real time
Exposure to rehabilitation technology integration, including assistive devices, digital interfaces, or adaptive control systems
Experience supporting multi-site clinical studies or working directly with investigators and study coordinators
Comfort working with data systems (e.g., EDC platforms, basic data visualization tools) to review participant performance and study metrics
Understanding of usability, human factors, and patient-centered design principles
Prior involvement in training clinicians or participants on device use and workflows
Experience working in early-stage or rapidly evolving clinical programs where processes are still being defined
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$89,000 - $250,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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Global Supply Manager
Neuralink · Austin, Texas, United States
Pay
$68k–177k
Setting
On-site
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Global Supply Manager
Austin, Texas, United States; South San Francisco, California, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
About the Team
The Supply Chain organization owns the external manufacturing and supplier network behind every component of our products. Global Supply Managers (GSMs) own the commercial relationship with our supplier base — from supplier identification and selection, through contract negotiation, cost management, capacity commitments, and ongoing business performance. GSMs partner day-to-day with Supplier Industrialization Engineering (SIE), Quality, Design Engineering, Manufacturing, Planning, and Finance to make sure Neuralink has the right suppliers, on the right terms, delivering the right parts, on the right schedule.
About the Role
As a Global Supply Manager, you will own the commercial strategy and performance of a portfolio of suppliers spanning the full breadth of what goes into the Implant and the Robot. This is explicitly a generalist role: rather than specializing in a single commodity, you will move across machined parts, molded plastics, electromechanical assemblies, PCBAs, raw materials, optics, hermetic packaging, coatings, and biocompatible materials — going wherever the business needs the most commercial leverage. You will drive sourcing strategy, negotiate contracts and pricing, manage supplier performance, and be the single point of accountability for the commercial health of your portfolio.
We expect generalists to be biased toward learning new categories rapidly, comfortable owning commodities they have not personally sourced before, and willing to develop the technical fluency required to negotiate credibly with engineering-led suppliers.
We are hiring across multiple levels. Early-career GSMs will own a focused portfolio under mentorship; senior and staff GSMs will own multi-commodity strategy across both programs, lead the most complex negotiations, and shape Neuralink’s long-term supply-base architecture.
What You'll Do
Sourcing Strategy & Supplier Selection
Own end-to-end sourcing strategy for a portfolio of categories spanning mechanical, electromechanical, electronic, optical, raw-material, and biocompatible-material commodities used in the Implant and Robot. Drive technical and commercial requirement definition, supplier evaluation, scoring, and award recommendation.
Identify, qualify, and onboard new suppliers; build a global, resilient supplier base with deliberate dual-sourcing and geographic-risk strategies.
Contracts & Cost Management
Negotiate contracts, MSAs, statements of work, NDAs, quality agreements, and IP terms in partnership with Legal and Finance — in a way that protects Neuralink's IP and regulatory position without strangling supplier flexibility.
Build should-cost models and total-cost-of-ownership analyses; lead year-over-year cost reduction (VAVE, resourcing, redesign, payment-term, freight, and yield levers). Own pricing negotiation for material and services impacting the manufacturing of Neuralink’s products
Partner with Design and SIE teams on Design for Manufacturability, Design for Cost, and make/buy decisions early in the development cycle — not after the design is frozen.
Supplier Performance & Capacity
Manage supplier performance against quality, delivery, cost, and responsiveness scorecards; lead quarterly business reviews (QBRs) and drive corrective action when performance slips.
Own capacity planning and capacity commitments with suppliers; align supplier capacity to Neuralink's clinical-build and commercial-ramp forecasts, including upside scenarios.
Be the commercial single point of accountability when a supply issue threatens a clinical or commercial build — from first escalation through closed recovery.
Risk & Continuity Management
Drive supply-risk management: map sub-tier dependencies, monitor geopolitical and financial-health risk, and build mitigation plans (inventory buffers, dual-source, alternate qualifications).
Manage end-of-life and obsolescence for sourced components; ensure transitions to replacement parts are planned, qualified, and commercially closed before supply gaps occur.
Required Qualifications
Background & Experience
Bachelor's degree in a technical or business discipline — Engineering (Mechanical, Electrical, Industrial, Manufacturing, Materials, Chemical, Biomedical, or Aerospace), Supply Chain Management, Operations, Business, Finance, or Economics — or equivalent practical experience demonstrating the same analytical depth.
Generalist track record: demonstrated experience moving across at least two distinct commodities or categories, learning new technical and commercial domains quickly rather than specializing in a single category throughout your career.
Sourcing and supplier management experience in one or more of: hardware manufacturing, medical devices, aerospace, automotive, consumer electronics, semiconductor, robotics, industrial OEM, or military/government/consulting environments that develop the same skill set.
Sourcing & Negotiation
Hands-on experience running full RFI/RFQ/RFP cycles end-to-end — from requirements definition and supplier scorecarding through award, contract execution, and supplier onboarding.
Demonstrated commercial negotiation experience across piece-price, tooling, NRE, payment terms, lead time, MOQ, capacity commitments, and IP/liability terms; comfortable holding the line with suppliers without burning the relationship.
Strong should-cost and total-cost-of-ownership analytical skills, including the ability to build a cost model from material, process, labor, overhead, yield, and margin inputs and use it to drive negotiation outcomes.
Supplier Quality & Industrialization
Working familiarity with the supplier-quality and industrialization toolkit (PPAP, APQP, FAI, PFMEA, FMEA, control plans, SPC, MSA, 8D/RCCA) — enough to operate credibly with SIE and Quality counterparts and to read a supplier's process documents.
Working familiarity with at least one Quality Management System framework — ISO 13485, 21 CFR Part 820, AS9100, IATF 16949, or ISO 9001 — and how it shapes change control, documentation, and supplier qualification.
Technical & Commercial Literacy
Solid technical literacy: able to read engineering drawings, basic GD&T, BOMs, and bills of process; able to translate between engineering and commercial language without losing fidelity in either direction.
Contract literacy: practical experience reading and redlining MSAs, supply agreements, quality agreements, NDAs, and statements of work in partnership with Legal — with a clear sense of what matters commercially and what matters legally.
Familiarity with ERP and procurement systems (e.g., NetSuite, SAP, Oracle, Coupa, Ariba, Zip) and an understanding of how data flows from BOM to PO to receipt to payment.
Execution & Communication
Strong project-management skills: able to run a parallel portfolio of sourcing initiatives against aggressive dates, sequence dependencies, escalate cleanly, and communicate status to stakeholders without being chased.
Strong written and verbal communication: able to run a supplier negotiation, walk an engineering team through a make-vs.-buy tradeoff, and write a one-page recommendation for leadership — all in the same day.
Strong financial and data fluency: comfortable in Excel/Google Sheets for cost modeling and scenario analysis.
Comfortable in a hands-on, fast-moving, ambiguity-tolerant environment where you are expected to own commercial outcomes, not just process — and to make sound decisions with incomplete information.
Logistics
Willingness to travel up to 25–50% to supplier sites, including international travel; valid passport (or ability to obtain one) required.
Must be able to work on-site in Austin, TX or South San Francisco, CA.
Preferred Qualifications
Advanced Education
MBA, MS in Supply Chain/Operations, or equivalent advanced education.
Regulated & Complex Hardware Experience
Sourcing experience in a regulated medical-device environment (ISO 13485/21 CFR Part 820), implantable hardware, or precision medical instruments.
Direct experience scaling a complex hardware product from clinical/pre-production builds through commercial volume — i.e., the full Design → Qualify → Scale → Sustain → End-of-Life lifecycle.
Prior experience at a high-growth, fast-paced hardware company.
Experience structuring dual-source and second-source qualifications, including the commercial choreography of running them in parallel with engineering qualification.
Experience with supplier-development and supplier-financial-health monitoring (D&B, RapidRatings, supplier audits) and with managing distressed-supplier situations.
International & Cross-Cultural Experience
Experience negotiating with suppliers internationally (APAC, EU, MX) and managing cross-cultural commercial relationships; second-language ability (Mandarin, German, Japanese, Spanish) a plus.
Certifications & Compliance
Lean/Six Sigma certification (Green Belt or higher), CPSM, CSCP, or equivalent.
Familiarity with U.S. export-control regimes (ITAR, EAR) and medical-device-specific regulatory frameworks (FDA QSR, EU MDR) as they touch the supply chain.
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$68,000 - $177,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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Software Engineer, CI/CD
Neuralink · Austin, Texas, United States
Pay
$123k–216k
Setting
On-site
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Software Engineer, CI/CD
Austin, Texas, United States; South San Francisco, California, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Infrastructure Team builds the foundation that enables the company to operate safely, robustly, and move at light-speed. We run a mixture of cloud-based and on-prem systems and have a user base spanning from highly technically proficient engineers to non-technical scientists and doctors; but all of them need solid systems, rugged networking, and bullet-proof software to do their jobs.
Job Responsibilities and Description:
As a Software Engineer, CICD you will integrate tightly with teams across the company, and span all layers of the work environment stack, from deployment of physical hardware on the manufacturing line, to custom tooling to stream neural recordings from implants. You will:
Design and scale the CI/CD platform that enables engineering teams to ship safely and quickly across verticals including, but not limited to, Brain Implant, Surgical Robot, BCI App, Clinical, Full-stack services and infrastructure
Own the software/firmware build tooling at scale. This includes remote caching, remote execution, target identification and selection, etc.
Operate and scale a runner fleet spanning on-prem and cloud clusters, cover multiple hardware platforms including Mac, Linux, Embedded devices and Hardware-in-the-loop fixtures
Maintain reproducible build and CI environments with Nix
Instrument CI health with Prometheus metrics, Grafana dashboards, and automated alerting to maintain high signal-to-noise on pipeline reliability
Reduce developer cycle time through pre-commit tooling, caching strategies, test sharding, and build graph optimization
Tech Stack:
Rust, Python
Terraform
Bazel and Nix
Kubernetes
GitLab CI
AWS
Darwin, Ubuntu, Fedora
Required Qualifications:
Deep experience operating Bazel, or similar hermetic build systems
Hands-on experience operating Kubernetes
Production experience with GitLab CI (or comparable CI platform), including pipeline architecture, runner fleet management, and custom executor integrations
Expertise in operating UNIX systems, including Linux and Mac
Familiarity with Nix for reproducible environments, or equivalent experience ensuring hermetic, cacheable builds
Bachelor's degree in computer science, a related field, or an equivalent combination of education, training, and/or experience
Preferred Qualifications:
Familiarity with hardware in the loop testing setups
Experience working with build system and CI tooling in a monorepo context
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$123,000 - $216,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.
Electrical Engineer, Implant Embedded Systems
Neuralink · Austin, Texas, United States
Pay
$110k–238k
Setting
On-site
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Electrical Engineer, Implant Embedded Systems
Austin, Texas, United States; South San Francisco, California, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
We build the electrical systems that make high-bandwidth brain–computer interfaces possible. This includes neural signal acquisition and stimulation to wireless power delivery, embedded processing, and system integration—all within devices small enough to be implanted in the human body and efficient enough to operate under strict thermal and power constraints. Our work sits at the intersection of analog, RF, digital, and biological systems. Many problems in this space do not present clean abstractions or clear failure modes. Success often depends on careful measurement, iteration, and engineering judgment across multiple interacting systems.
Job Responsibilities:
Utilize electrical engineering fundamentals and best system design practices to deliver high-performant, reliable, and manufacturable extremely size-constraint systems
Contribute to all phases of system and board design, from system definition to part selection, schematic design, layout, bring up, and design verification
Help conduct R&D investigations and experiments to demonstrate feasibility of new technology for the implant and the charger
Work cross functionally to ensure successful systems integration
Contribute to system improvements that decrease latency and increase battery life, reliability, and safety
Design and deploy systems for implant-charger hardware in the loop testing, and manufacturing line quality control
Note: The team is hiring electrical engineers at all levels, both junior and senior. What matters most is evidence of exceptional abilities and a drive to succeed.
Required Qualifications:
Bachelor’s degree in Electrical Engineering or equivalent experience
Strong electrical engineering and physics fundamentals, with demonstrated ability to apply them under real-world constraints (noise, power, size, non-ideal interfaces)
Proven ability to independently design, bring up, debug, and verify complex PCBAs operating under tight power and size constraints, including mixed-signal circuits, sensitive sensor interfaces, and embedded compute
Experience debugging systems where issues span multiple domains (analog, digital, RF, power) and root causes are not immediately obvious
Deep familiarity with lab instrumentation (oscilloscopes, power supplies, spectrum analyzers, VNAs) and the ability to extract meaningful insight from imperfect measurements
Preferred Qualifications:
Experience shipping highly integrated, size- and power-constrained devices (e.g., wearables, implantables, compact wireless systems)
Experience with wireless systems and RF design tradeoffs (BLE, Wi-Fi, antenna design, coexistence)
Experience supporting hardware through manufacturing at scale, including yield, test, and failure analysis
Experience in safety-critical or regulated environments, where reliability and risk must be explicitly managed
Familiarity with mechanical integration constraints (CAD tools, packaging, stack-ups)
Experience with electromagnetic simulation and antenna validation (FEM/FDTD or equivalent)
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$109,800 - $238,100 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.
Clinical Scientist
Neuralink · Austin, Texas, United States
Pay
$108k–200k
Setting
On-site
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Clinical Scientist
Austin, Texas, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what’s possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink’s BCI technology for use in people!
Job Description and Responsibilities:
As a Clinical Scientist I, you will support the development, design, and execution of Neuralink’s clinical evidence strategy. This role focuses on translating product and research objectives into clinical study designs, supporting data analysis, and ensuring scientific rigor across clinical programs.
This individual is a self-driven and analytically strong individual who can contribute to clinical strategy while executing with precision. The ideal contributor is detail-oriented, collaborative, and comfortable working in a fast-paced, multidisciplinary environment.
In this role, you will:
Support the design and development of clinical study protocols, including endpoints, inclusion/exclusion criteria, and statistical considerations
Contribute to clinical strategy by translating research and product goals into evidence-generating study plans
Partner with other team members to support execution of clinical studies and ensure alignment between scientific intent and operational delivery
Build and maintain strong working relationships with internal teams, investigators, and external partners
Support preparation of study-related documents, including protocols, investigator brochures, clinical study reports, and regulatory submissions
Contribute to EDC and CRF design by ensuring alignment between protocol objectives, endpoints, and data collection strategy
Translate clinical and scientific requirements into structured, high-quality data capture and validation approaches
Assist in data review, analysis, and interpretation to evaluate safety and performance outcomes
Contribute to development of abstracts, presentations, and publications
Support interactions with ethics committees (e.g., IRB, RECs) and regulatory bodies as needed
Ensure scientific and clinical activities are conducted in compliance with Good Clinical Practice (GCP), applicable regulations, and internal SOPs
Identify data trends, inconsistencies, or risks and proactively communicate findings to the broader team
Required Qualifications:
Familiarity with statistical methods or programming (e.g., Python, R)
5+ years of experience in clinical research or scientific roles within medical devices or related fields
Strong analytical and problem-solving skills with the ability to interpret complex data
Familiarity with clinical study design, endpoints, and data analysis concepts
Working knowledge of Good Clinical Practice (GCP) and basic regulatory requirements (e.g., ISO 14155)
Ability to work cross-functionally with clinicians, engineers, and operational teams
Strong written and verbal communication skills, particularly in scientific and technical contexts
High attention to detail and ability to manage multiple priorities
Preferred Qualifications:
Experience with neurological, neurosurgical, or implantable medical device studies
Experience supporting protocol development, data analysis, or clinical reporting
Publications or scientific presentations in biomedical engineering or neuroscience
PhD in neuroscience, biomedical engineering, or a related field
Additional Requirements and Competencies:
Willingness to travel (up to ~20–30%) to support site visits, investigator meetings, and study activities
Strong organizational and documentation skills
Ability to work independently while collaborating closely with cross-functional teams
Adaptability and comfort in a fast-paced, high-growth environment
Commitment to scientific rigor, patient safety, and high-quality evidence generation
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$108,000 - $200,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.
Prototype & Design Specialist
Neuralink · Austin, Texas, United States
Pay
$68k–114k
Setting
On-site
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Prototype & Design Specialist
Austin, Texas, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Brain Interfaces Team is responsible for the design, manufacturing, and testing of all systems related to the implant and charger. Our projects involve electrical and mechanical test systems, custom jigs and fixtures, electronics packaging and tooling at the interface between the implant and the surgical robot.
Job Description and Responsibilities:
As our Prototype & Design Specialist, you will be instrumental in creating and maintaining an environment that enables our engineering and manufacturing teams to innovate and deliver groundbreaking medical devices. You will go beyond managing equipment and facilities; you will be a key enabler of technical and operational success, ensuring that the R&D lab spaces are designed for efficiency and collaboration. You will play a pivotal role in supporting the company’s growth by facilitating innovation, streamlining operations, and optimizing resource utilization. Additionally, you will be expected to:
Engineering Lab Design and Operations:
Design and build lab spaces to meet the evolving needs of the engineering and manufacturing teams
Continuously improve lab capabilities and operations by implementing new technologies and optimizing space for faster and more efficient workflows
Own and maintain inventory of all lab equipment, including tools, chemicals, and consumables
Implement systems for lab organization and cleanliness, and train users accordingly
Ensure spaces comply with safety regulations and industry standards
Prototyping and Fabrication:
Provide hands-on technical support to engineers and technicians by building prototypes, setting up stations and running tests
Utilize various fabrication methods, including additive and subtractive manufacturing, to produce high-quality prototype parts.
Operate and maintain a range of machines and power/hand tools necessary for prototyping
Manage multiple projects simultaneously, prioritizing tasks to meet tight deadlines and production schedules
Required Qualifications:
Meticulous attention to detail and exceptional organizational skills
Eye for aesthetic design and organization
Familiarity with R&D lab equipment, tools and workflows
Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams
Thrives in a fast-paced environment where flexibility and innovation are essential
Hands-on experience with prototyping, model making, fabrication, testing, and lab operations
Experience planning and building out labs and R&D workspaces
Preferred Qualifications:
Previous experience in a prototyping environment
Part design experience
Experience programming and operating laser cutters, 3D printers, and CNC machines
Knowledge of regulatory standards relevant to medical device development
Experience with inventory management systems and quality control processes
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$68,000 - $114,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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This is your opportunity to showcase why you will be an exceptional fit for this specific role. Please provide an example of when you have managed, designed, or created an R&D lab or workshop environment.*
Please provide two examples showcasing your ability to create impressive parts, assemblies, or prototypes. (What parts did you make, how did you make them, why was it challenging?)*
Please provide an example showcasing your extreme attention to detail and love for all things organization (ideally in the context of an R&D environment).*
Why is this position a perfect fit for you?
What about being a Prototype & Design Specialist excites you?
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Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.
Prototyping Lab Engineer & Manager
Neuralink · Austin, Texas, United States
Pay
$68k–114k
Setting
On-site
Back to jobs
Prototyping Lab Engineer & Manager
Austin, Texas, United States
Apply
About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Brain Interfaces Team is responsible for the design, manufacturing, and testing of all systems related to the implant and charger. Our projects involve electrical and mechanical test systems, custom jigs and fixtures, electronics packaging and tooling at the interface between the implant and the surgical robot.
Job Description and Responsibilities:
As our Prototyping Lab Engineer & Manager, you will be instrumental in creating and maintaining an environment that enables our engineering and manufacturing teams to innovate and deliver groundbreaking medical devices. You will go beyond managing equipment and facilities; you will be a key enabler of technical and operational success, ensuring that the R&D lab spaces are designed for efficiency and collaboration. You will play a pivotal role in supporting the company’s growth by facilitating innovation, streamlining operations, and optimizing resource utilization. Additionally, you will be expected to:
Engineering Lab Design and Operations:
Design and build lab spaces to meet the evolving needs of the engineering and manufacturing teams
Continuously improve lab capabilities and operations by implementing new technologies and optimizing space for faster and more efficient workflows
Own and maintain inventory of all lab equipment, including tools, chemicals, and consumables
Implement systems for lab organization and cleanliness, and train users accordingly
Ensure spaces comply with safety regulations and industry standards
Prototyping and Fabrication:
Provide hands-on technical support to engineers and technicians by building prototypes, setting up stations and running tests
Utilize various fabrication methods, including additive and subtractive manufacturing, to produce high-quality prototype parts.
Operate and maintain a range of machines and power/hand tools necessary for prototyping
Manage multiple projects simultaneously, prioritizing tasks to meet tight deadlines and production schedules
Required Qualifications:
Meticulous attention to detail and exceptional organizational skills
Eye for aesthetic design and organization
Familiarity with R&D lab equipment, tools and workflows
Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams
Thrives in a fast-paced environment where flexibility and innovation are essential
Hands-on experience with prototyping, model making, fabrication, testing, and lab operations
Experience planning and building out labs and R&D workspaces
Preferred Qualifications:
Previous experience in a prototyping environment
Part design experience
Experience programming and operating laser cutters, 3D printers, and CNC machines
Knowledge of regulatory standards relevant to medical device development
Experience with inventory management systems and quality control processes
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$68,000 - $114,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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This is your opportunity to showcase why you will be an exceptional fit for this specific role. Please provide an example of when you have managed, designed, or created an R&D lab or workshop environment.*
Please provide two examples showcasing your ability to create impressive parts, assemblies, or prototypes. (What parts did you make, how did you make them, why was it challenging?)*
Please provide an example showcasing your extreme attention to detail and love for all things organization (ideally in the context of an R&D environment).*
Why is this position a perfect fit for you?
What about being a Prototyping Lab Engineer & Manager excites you?
Please link or attach your professional portfolio.*
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I have hands-on experience with prototyping, fabrication, and testing.*
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Are you currently authorized to work in the United States?*
Select...
Will you, at any point, require employer sponsorship to work in the United States?*
Select...
I am willing and able to work entirely on-site.*
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I will need relocation to work on-site.*
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How did you hear about us?*
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Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.
Engineering Lab Manager
Neuralink · Austin, Texas, United States
Pay
$68k–114k
Setting
On-site
Back to jobs
Engineering Lab Manager
Austin, Texas, United States
Apply
About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Brain Interfaces Team is responsible for the design, manufacturing, and testing of all systems related to the implant and charger. Our projects involve electrical and mechanical test systems, custom jigs and fixtures used in manufacturing and assembly, electronics packaging, and tooling at the interface between the implant and the surgical robot.
Job Description and Responsibilities:
As an Engineering Lab Manager, you will be instrumental in creating and maintaining an environment that empowers our engineering and manufacturing teams to innovate and deliver groundbreaking medical devices. You will go beyond managing equipment and facilities; you will be a key enabler of technical and operational success, ensuring that the lab spaces are designed for efficiency and collaboration. You will play a pivotal role in supporting the company’s growth by facilitating innovation, streamlining operations, and optimizing resource utilization. Additionally, you will be expected to:
Collaborate with stakeholders in the design and optimization of spaces to meet the evolving needs of the engineering and manufacturing teams
Continuously improve lab capabilities and operations by implementing new technologies, optimizing space for better workflow, or renovating existing facilities
Maintain and manage inventory of all lab equipment, including tools, chemicals, and consumables
Proactively implement maintenance strategies and deliver systems for lab organization and cleanliness as well as train users accordingly
Build prototypes, run tests and experiments, and provide hands-on technical support to engineers, leveraging expertise in engineering, prototyping, and lab operations
Ensure spaces comply with safety regulations and industry standards
Required Qualifications:
Meticulous attention to detail and exceptional organizational skills
Strong understanding of engineering principles and familiarity with R&D lab equipment
Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams
Thrives in a fast-paced environment where flexibility and innovation are essential
Hands-on experience with prototyping, testing, and lab operations
Preferred Qualifications:
Knowledge of regulatory standards relevant to medical device development
Experience with inventory management systems and quality control processes
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$68,000 - $114,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
Create a Job Alert
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Phone*
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Cover Letter
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Accepted file types: pdf, doc, docx, txt, rtf
This is your opportunity to showcase why you will be an exceptional fit for this specific role. Please provide an example of when you have managed, designed, or created an R&D lab or workshop environment.*
Please provide two examples showcasing your ability to create impressive parts, assemblies, or prototypes. (What parts did you make, how did you make them, why was it challenging?)*
Please provide an example showcasing your extreme attention to detail and love for all things organization (ideally in the context of an R&D environment).*
What about being an Engineering Lab Manager excites you?
Why is this position a perfect fit for you?
Please link or attach your professional portfolio.*
Additional Attachment
Attach
Attach
Dropbox
Google Drive
Accepted file types: pdf, doc, docx, txt, rtf
Are you currently authorized to work in the United States?*
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Will you, at any point, require employer sponsorship to work in the United States?*
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I am willing and able to work entirely on-site.*
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I will need relocation to work on-site.*
Select...
Ideal start date in office*
How did you hear about us?*
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Please specify
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Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.
Microfabrication Technician (Second Shift)
Neuralink · Fremont, California, United States
Pay
$28.76/hr
Setting
On-site
Back to jobs
Microfabrication Technician (Second Shift)
Fremont, California, United States
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About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Microfabrication Team, a division of the Brain Interfaces Hardware Department, designs, manufactures, and verifies the thin-film microelectrode array that records and relays neural signals to the body of the implant. The team operates at an in-house cleanroom facility in Fremont, with operations expanding to Austin in the near future.
Job Description and Responsibilities:
As a Microfabrication Technician (Second Shift) at Neuralink, you will be responsible for the production of our thin-film microelectrode arrays, collaborating with engineers to maintain equipment and processes within specification, and working to improve array throughput. As such, you will be instrumental in ramping production and accelerating Neuralink’s progress.
Note: Second shift schedule will be 6 pm to 2 am, Monday through Friday.
Additional responsibilities will include:
Operating equipment such as ASML, photoresist spin coater, reactive ion etcher, e-beam evaporator, sputter physical vapor deposition system, plasma enhanced chemical vapor deposition, and wet processing stations
Troubleshooting and maintaining equipment and equipment calibration and performance
Creating and maintaining process documentation and equipment documentation, including daily process logs and equipment logs
Actively collecting data and visually detecting defects on production lines in a fast-paced environment
Assisting in data analysis of throughput, quality, and repeatability of manufacturing processes
Ensuring product quality and conformance to design requirements
Collaborating with engineers to refine, troubleshoot, and improve processes while maintaining or enhancing product quality and yield
Keeping a clean, organized, and thoroughly-maintained cleanroom or workspace
Testing the finished thin-film arrays to ensure that they meet the required specifications or standards
Required Qualifications:
High school diploma or equivalent
Excellent verbal and written communication
Resourceful, flexible, and adaptable; no task is too big or too small
Strong self-discipline and organizational skills
Ability to work in a medical device regulatory environment
Ability to thrive in a dynamic and constantly changing environment
Ability to work 6 pm to 2 am Monday through Friday, ending on Saturday morning
Preferred Qualifications:
2+ years of hands-on experience working in a cleanroom or lab where precision is critical
Solid understanding of basic physics and engineering fundamentals
Demonstrated ability to interpret, distill, and disseminate relevant technical information
Additional Requirements and Competencies:
Ability to travel to and work at other manufacturing locations such as Austin, Texas
Ability to lift and transfer up to 25 pounds
Ability to spend long periods standing and walking within a cleanroom environment
Ability to work 6 pm to 2 am, Monday through Friday
Expected Compensation:
At Neuralink, your base pay is one part of your total compensation package. The anticipated hourly rate for this position is expected to be within the below range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training.
California Hourly Range:
$28.76/Hr USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Paid holidays
Commuter benefits
Meals provided
Equity (RSUs) *Temporary Employees & Interns excluded
401(k) plan *Interns initially excluded until they work 1,000 hours
Parental leave *Temporary Employees & Interns excluded
Flexible time off *Temporary Employees & Interns excluded
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Ability to work reliably with small and delicate components where precision is critical
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