Chemist

Neuralink•Austin, TX

3d•Onsite

About The Position

Neuralink is creating devices that enable a bi-directional interface with the brain, aiming to restore movement to the paralyzed, sight to the blind, and revolutionize human interaction with the digital world. The Biocompatibility Team is responsible for executing a wide range of assays, performing method validations, finalizing reports, and supporting R&D activities. This team comprises skilled professionals dedicated to ensuring the accuracy, reliability, and regulatory compliance of test methods used in quality control. With expertise in analytical techniques like chemical characterization, microbiological testing, and biocompatibility evaluations, as well as manufacturing processes such as cleaning, sterilization, and passivation, the team is crucial for maintaining high standards of product quality and patient safety.

Requirements

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.

Nice To Haves

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.

Responsibilities

Collaborate with cross-functional teams across Neuralink to analyze the chemical and biological characteristics of manufacturing processes and finished devices.
Perform various levels of product testing during R&D and product release to generate data required for regulatory approvals, confirming patient safety in accordance with applicable global regulations, regulatory guidelines, and voluntary consensus standards.
Draft internal procedures and test protocols.
Prepare test samples and controls for analysis.
Perform chromatographic and mass spectrometric analysis using instruments such as LC-MS, GC-MS, and ICP-MS.
Conduct 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.
Deliver test results related to device characteristics to support manufacturing changes and risk assessments.
Prepare laboratory reports that comply with applicable medical device evaluation standards and FDA/ISO guidance documents within a risk-based framework.
Collaborate with cross-functional teams to support multiple projects, ensuring timely completion of laboratory deliverables to meet project timelines.
Analyze test results to determine whether data meets internal and external requirements; utilize problem-solving skills and technical expertise to troubleshoot unexpected outcomes.
Participate in continuous improvement initiatives to increase laboratory efficiency, reduce turnaround times, and enhance data quality.
Manage laboratory inventory and perform other general laboratory tasks.