Connecting brains and machines for a better future
Neuralink, headquartered in Fremont, CA, is pioneering ultra-high bandwidth brain-machine interfaces aimed at restoring autonomy for individuals with paralysis. With $1.3 billion raised in Series D funding, the company has completed human trials after securing FDA approval in 2023, marking a signifi...
Neuralink offers excellent medical, dental, and vision insurance through a PPO plan, flexible time off, and paid holidays. Employees also benefit from...
Neuralink fosters a culture of innovation and ambition, focusing on groundbreaking technology that merges neuroscience with engineering. The company v...
Neuralink • Austin, Texas, United States
Neuralink is hiring a Quality Assurance Specialist to ensure compliance with regulatory standards in the development of innovative brain interface devices. You'll work closely with various teams to maintain quality control and adherence to protocols. This role requires experience in quality assurance and regulatory compliance.
You have a strong background in quality assurance, ideally with experience in regulatory compliance within the medical or technology sectors. You understand the importance of adhering to ISO standards and Good Laboratory Practices (GLP), and you are skilled in maintaining meticulous documentation and protocols. Your problem-solving abilities allow you to navigate complex compliance challenges effectively, ensuring that all processes meet the necessary standards. You are detail-oriented and possess excellent communication skills, enabling you to convey findings clearly to management and team members.
Experience in a fast-paced environment where you have contributed to quality assurance processes in a clinical or laboratory setting is a plus. Familiarity with auditing practices and the ability to perform inspections will enhance your candidacy. You are proactive in identifying areas for improvement and have a collaborative mindset that fosters teamwork.
As a Quality Assurance Specialist at Neuralink, you will play a crucial role in ensuring that all regulatory standards are met throughout the development process of our groundbreaking devices. You will maintain copies of all approved protocols and manage a master schedule of GLP-regulated studies. Your responsibilities will include performing pre-qualification inspections of testing facilities and providing periodic status reports to management regarding compliance and quality control. You will inspect and audit processes to ensure data integrity and verify compliance with established protocols. Communicating your findings through signed inspection reports will be essential to maintaining transparency and accountability within the team.
At Neuralink, we provide a supportive work environment that values innovation and collaboration. You will have access to excellent medical, dental, and vision insurance, along with paid holidays and commuter benefits. We also offer equity options and a 401(k) plan to help you plan for your future. Our flexible time-off policy allows you to balance your work and personal life effectively. Join us in our mission to revolutionize how humans interact with technology and make a meaningful impact on the world.
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