About Neuralink
Connecting brains and machines for a better future
Key Highlights
- Secured FDA approval in 2023 for human trials
- Raised $1.3 billion in Series D funding
- Headquartered in Fremont, CA with 501-1000 employees
- Developing brain-machine interfaces to assist those with paralysis
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...
🎁 Benefits
Neuralink offers excellent medical, dental, and vision insurance through a PPO plan, flexible time off, and paid holidays. Employees also benefit from...
🌟 Culture
Neuralink fosters a culture of innovation and ambition, focusing on groundbreaking technology that merges neuroscience with engineering. The company v...
Overview
Neuralink is hiring a GLP Quality Assurance Specialist to ensure compliance with regulatory standards and optimize performance in their quality assurance processes. You'll work closely with teams to maintain protocols and conduct inspections. This role requires a strong commitment to quality and compliance.
Job Description
Who you are
You have experience in quality assurance and a strong understanding of regulatory standards, particularly in the context of GLP and ISO compliance. You thrive in environments that require attention to detail and a commitment to continuous improvement. Your problem-solving skills enable you to identify gaps and implement effective systems that drive compliance and optimize performance.
You are passionate about quality assurance and understand the importance of maintaining high standards in regulated processes. You have a collaborative mindset and enjoy working with cross-functional teams to ensure that all protocols are followed and that the quality of work meets or exceeds expectations. Your ability to communicate findings clearly to management and study directors is a key strength.
What you'll do
As a GLP Quality Assurance Specialist at Neuralink, you will be responsible for ensuring that all regulatory standards are adhered to within the organization. This includes maintaining copies of all approved protocols and managing a master schedule of GLP-regulated studies. You will perform pre-qualification inspections of testing facilities as needed and provide periodic status reports to management regarding facility compliance and quality control.
You will inspect and audit studies at critical phases, communicating your findings to the appropriate management teams. Your role will involve collaborating with various teams to ensure that quality assurance processes are effectively implemented and maintained. You will play a crucial role in setting internal quality standards that exceed FDA expectations, contributing to the overall mission of Neuralink to revolutionize how humans interact with their digital world.
What we offer
Neuralink provides a supportive work environment with excellent medical, dental, and vision insurance through a PPO plan. You will enjoy paid holidays, commuter benefits, and meals provided at the office. Additionally, we offer equity (RSUs) and a 401(k) plan, along with flexible time off policies. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse backgrounds and perspectives.
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