Neuralink
Overview
Toxicologist role at Neuralink focused on leading toxicological risk assessments and biocompatibility evaluations to advance the safety of brain‑computer interface technologies. This role offers the opportunity to own key processes in a collaborative, fast‑paced environment focused on innovative medical devices, while ensuring alignment with regulatory standards like ISO 10993 and FDA guidelines.
Responsibilities
Prepare toxicological risk assessment reports, biological safety evaluations, and contribute to FDA and international regulatory submissions
Own toxicological risk assessment (TRA), including developing and documenting standard operating procedures (SOPs) that outline the TRA process and utilizing risk assessment tools such as the QSAR toolbox, read‑across methodologies, and other risk assessment resources
Conduct hazard identification, literature reviews, and dose‑response assessments to support TRA
Interpret chemical characterization data in accordance with ISO 10993 standards and integrate findings into comprehensive biocompatibility assessments for medical devices
Collaborate with engineering teams to provide expert consultation on the selection of materials and chemical agents used in manufacturing processes
Lead the development, validation, and ongoing sustainment of in‑vitro biocompatibility assays, ensuring reproducibility, appropriate endpoints, and compliance with international guidance
Support general laboratory operations, including equipment management, calibration, and routine maintenance tasks to maintain a safe and efficient workspace
Required Qualifications
B.S. in toxicology, pharmacology, biochemistry, or a related field
>1 year of experience in toxicological risk assessment, preferably in the medical device or pharmaceutical industries
Proficiency in risk assessment methodologies and tools, such as QSAR modeling and read‑across
Excellent analytical, problem‑solving, and communication skills, with the ability to collaborate across interdisciplinary teams
Ability to conduct thorough literature searches
Preferred Qualifications
M.S. or PhD in toxicology, pharmacology, biochemistry, or a related field
Strong knowledge of ISO 10993 standards and experience with chemical characterization and biocompatibility evaluations
Hands‑on experience with in‑vitro assay development and cell culture techniques
>3 years of experience in toxicological risk assessment, preferably in the medical device industry or pharmaceutical industry
Certification as a Diplomate of the American Board of Toxicology (DABT) or similar professional credential
Familiarity with FDA and international regulatory submissions
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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Responsibilities
Prepare toxicological risk assessment reports, biological safety evaluations, and contribute to FDA and international regulatory submissions
Own toxicological risk assessment (TRA), including developing and documenting standard operating procedures (SOPs) that outline the TRA process and utilizing risk assessment tools such as the QSAR toolbox, read‑across methodologies, and other risk assessment resources
Conduct hazard identification, literature reviews, and dose‑response assessments to support TRA
Interpret chemical characterization data in accordance with ISO 10993 standards and integrate findings into comprehensive biocompatibility assessments for medical devices
Collaborate with engineering teams to provide expert consultation on the selection of materials and chemical agents used in manufacturing processes
Lead the development, validation, and ongoing sustainment of in‑vitro biocompatibility assays, ensuring reproducibility, appropriate endpoints, and compliance with international guidance
Support general laboratory operations, including equipment management, calibration, and routine maintenance tasks to maintain a safe and efficient workspace
Required Qualifications
B.S. in toxicology, pharmacology, biochemistry, or a related field
>1 year of experience in toxicological risk assessment, preferably in the medical device or pharmaceutical industries
Proficiency in risk assessment methodologies and tools, such as QSAR modeling and read‑across
Excellent analytical, problem‑solving, and communication skills, with the ability to collaborate across interdisciplinary teams
Ability to conduct thorough literature searches
Preferred Qualifications
M.S. or PhD in toxicology, pharmacology, biochemistry, or a related field
Strong knowledge of ISO 10993 standards and experience with chemical characterization and biocompatibility evaluations
Hands‑on experience with in‑vitro assay development and cell culture techniques
>3 years of experience in toxicological risk assessment, preferably in the medical device industry or pharmaceutical industry
Certification as a Diplomate of the American Board of Toxicology (DABT) or similar professional credential
Familiarity with FDA and international regulatory submissions
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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