Job Description and Responsibilities:Please note, this is a duplicate posting for the "Quality Systems Engineer" role. We are testing titling to see which attracts the most qualified candidates. Please only apply to one of the postings.
As a Software Design Controls Engineer, your primary responsibility will be to design, implement, and continuously improve software-focused design control systems with regulatory compliance embedded into their architecture.
You will build systems that eliminate ambiguity, reduce manual effort, and enable rapid and reliable development of regulated medical device software. These systems will support the full software lifecycle, from requirements definition through verification, validation, risk management, and release.
You will continuously optimize these systems to improve speed, traceability, and audit readiness while supporting aggressive development timelines and frequent design changes. Your responsibilities include, but are not limited to:
- Design and implement scalable software design controls systems aligned with IEC 62304 and FDA design control requirements (21 CFR 820.30)
- Develop and maintain end-to-end traceability frameworks linking:
- User needs
- Software requirements
- Risk controls
- Design outputs (code, architecture)
- Verification and validation evidence
- Integrate software risk management into design controls, ensuring alignment with ISO 14971 principles
- Build change control mechanisms capable of supporting:
- Rapid iteration
- Parallel development
- Same-day deployment
- Partner closely with software engineering teams to embed:
- Compliance with CI/CD pipelines
- Automated evidence generation
- Controlled release processes
- Own subsets of the Quality System related to software design controls, including but not limited to:
- Software Design Control processes
- Software Risk Management
- Software Change Control
- Software Verification & Validation traceability
Required Qualifications: - Bachelor's degree in Electrical Engineering, Computer Science, or a related technical field
- Demonstrated experience designing or maintaining structured engineering or compliance systems
- Familiarity with software development lifecycles in regulated or safety-critical environments
- Working knowledge of:
- Design Controls
- Software requirements management
- Proficiency in basic scripting, automation, or querying (e.g., Python, SQL, or equivalent)
- Excellent written and verbal communication skills
- Strong problem-solving mindset with the ability to think in systems rather than silos
Preferred Qualifications:- Familiarity with IEC 62304 (Medical Device Software Lifecycle Processes)
- Familiarity with FDA Design Controls (21 CFR 820.30)
- Familiarity with Design Risk Management (ISO 14971 principles)
- 1-3 years of experience in:
- Software Design Controls Engineer
- Software Quality
- Regulated software development
Expected 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
