Quality Assurance Specialist

About the Role

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. The Quality Assurance Team's mission is to ensure compliance with relevant regulatory standards and the functional, consistent, and reliable operation of our regulated processes.

Responsibilities

• Conduct audits of Good Laboratory Practice (GLP) activities within Neuralink, and when needed, assist with auditing Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and engineering activities, ensuring adherence to U.S. FDA regulatory requirements, any applicable international standards, and Neuralink policies
• Review evidence and issue findings for compliance concerns or deviations
• Determining that no deviations from approved protocols or standard operating procedures were made without proper authorization and/or documentation
• Communicate the findings of all QA inspections to appropriate management via signed inspection reports
• Assist with deviation and audit findings, tracking, ensuring their effective execution, and coordinating the timely closure of actions
• Assist with maintaining a master schedule of all GLP- regulated studies and copies of all approved protocols
• Assist with compliance initiatives and continuous quality improvement projects, as needed
• Ensure personnel training records are maintained by staff
• Assist with FDA inspections

Requirements

• Bachelor of Science degree, preferably in a science, engineering, or quality-related discipline
• Exposure to a regulated environment (e.g., FDA-regulated industry, GxP, ISO, or quality system work)
• Working knowledge of FDA regulatory requirements and standards
• Excellent communication and collaboration abilities
• Basic computer skills and proficiency in Google Docs, Google Drive, and Gmail
• Ability to travel to/from work in multistate locations

Preferred Qualifications

• Internship, co-op, or up to 1 year of experience in a medical device, pharmaceutical, or life sciences organization
• 1+ years of experience auditing
• 1+ year of experience within a regulatory environment
• Experience being part of external agency audits (e.g., FDA or other notified bodies)
• Experience following SOPs and documenting work accurately in a controlled process
• Working knowledge of the scientific method and engineering first principles
• Excellent organization and communication skills
• Keen eye for detail

Work Environment

Office, lab, operating room, and animal care facilities

Pay

The anticipated hourly rate for this position is expected to be within the range of $26.92 — $44.71/Hr USD, depending on job-related skills, experience, and relevant education or training.

Benefits

• 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)
• 401(k) plan
• Parental leave
• Flexible time off