Systems Verification & Test Engineer

Systems Verification & Test Engineer Huxley Medical, Inc. Atlanta, GA Job Details Full-time $75,000 - $105,000 a year 5 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Life insurance Referral program Qualifications Developing CAD designs Machine design Automation Bachelor's degree in engineering Bachelor's degree Organizational skills Design of mechanical systems Electrical Engineering Python Full Job Description Overview This is a unique opportunity to launch your career in systems engineering at a pivotal moment of growth. As demand accelerates, we're entering an exciting phase where scaling smart reliable systems is critical, and you can be part of building that foundation from the ground up. At Huxley, we're developing a category-defining diagnostic platform SANSA that brings together a wearable device, AI-powered cloud technology, and real-world medical workflows. Our work sits at the intersection of sleep medicine and cardiology, helping deliver meaningful insights that can improve patient outcomes. In this role, you'll work closely with experienced leaders and a team that has successfully built and scaled multiple companies. You'll gain hands-on experience across systems, operations, and product development, learning how complex technologies come together and scale in the real world. This is a great fit if you're curious, proactive, and excited to learn by doing. You'll have the chance to take ownership of real challenges, build practical skills quickly, and see the direct impact of your work as our product reaches more patients. Key Responsibilities Support product development documentation (requirements, risk, V&V matrices, product labeling) Execute V&V protocols for hardware, firmware, and system-level testing in accordance with regulatory standards Manage and coordinate outsourced testing and validation activities Support mechanical testing and design documentation using SolidWorks Develop and maintain automated test systems using Python and related tools Assist with new product introduction to manufacturing, including process documentation and training Support root cause investigations and corrective actions for sustaining products Collaborate with cross-functional teams including Quality, Operations, and Regulatory Requirements Bachelor's degree in Engineering (Electrical, Biomedical, Mechanical, or related field) Proficiency in Python scripting for automation and data analysis Hands-on experience with oscilloscopes, multimeters, and circuit-level debugging Proficiency with SolidWorks for mechanical design and drawing creation Strong communication, documentation, and organizational skills Nice to

Have:

3+ years of experience in the regulated medical device industry Familiarity with FDA Class II/III requirements and standards such as

ISO 13485, ISO 14971, IEC

60601, and

IEC 62304

• Compensation dependent on candidate experience.

Pay:

$75,000.00 - $105,000.00 per year

Benefits:

401(k) Dental insurance Health insurance Life insurance Paid time off Referral program Vision insurance

Work Location:

In person