Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers is dedicated to delivering prescription-grade therapy with an outstanding user experience. We have pioneered the world’s first drug-free wearable therapy, clinically proven to alleviate symptoms in adults with drug-resistant Restless Legs Syndrome (RLS). Be part of our mission to transform healthcare, improve lives, and drive meaningful change with Noctrix Health. 

We are seeking an experienced and innovative Principal Electrical Engineer to lead the architecture, design, and development of electrical systems supporting our next-generation therapeutic wearable devices. In this role, you will drive hardware innovation while ensuring designs meet the highest standards for safety, reliability, and performance within regulated medical device environments. 

The Principal Electrical Engineer will lead full lifecycle hardware development—from concept through manufacturing transfer—while collaborating with cross-functional teams to deliver high-quality, patient-centered products. This role reports to the SVP, Product and plays a critical role in shaping the technical direction of Noctrix Health’s hardware platforms. 

***This is a full-time, hybrid position located in our Pittsburgh office.*** 

Responsibilities: 

• Serve as the technical authority for electrical architecture and hardware design across Noctrix’s therapeutic wearable platforms. 
• Lead hands-on design and development of complex analog, digital, and mixed-signal circuits for medical device systems, including schematic capture, PCB layout oversight, and component selection. 
• Architect robust electrical systems that meet the performance, reliability, and safety requirements of prescription medical devices operating in FDA-regulated environments. 
• Drive full lifecycle hardware development—from early concept and feasibility through detailed design, verification, validation, and transfer to manufacturing. 
• Perform and guide detailed electrical engineering analysis including signal integrity, power management design, noise mitigation, and system-level performance optimization. 
• Lead rigorous troubleshooting and root cause investigations for electrical and system-level issues during development, verification testing, and manufacturing. 
• Develop, review, and maintain high-quality design documentation in compliance with medical device quality systems, including design inputs/outputs, risk analysis, verification protocols, and traceability artifacts. 
• Ensure electrical designs support regulatory compliance requirements including IEC 60601 safety, EMC, and applicable medical device standards. 
• Work closely with firmware and systems teams to develop integrated hardware solutions that deliver reliable therapeutic performance and exceptional patient experience. 
• Mentor engineers and contribute to raising the technical depth and engineering rigor of the hardware team. 
• Support manufacturing partners and internal teams in design for manufacturability (DFM), testability (DFT), and scale-up to production. 
• Contribute to the identification and development of new electrical technologies, architectures, and hardware platforms aligned with Noctrix’s long-term product roadmap 

Requirements: 

• B.S. in Electrical Engineering or equivalent technical discipline (M.S. preferred) 
• Minimum 15 years of experience designing and developing complex electrical systems, preferably in medical devices or other regulated industries (e.g., aerospace, automotive, industrial safety systems) 
• Deep expertise in analog, digital, and mixed-signal circuit design, including schematic capture, PCB layout guidance, and component selection 
• Strong proficiency with Altium Designer or similar professional PCB design tools 
• Demonstrated experience architecting and delivering battery-powered embedded systems, including power management, DC-DC conversion, Li-ion battery management, and charging circuitry 
• Experience designing systems using microcontrollers and embedded firmware interfaces, with working knowledge of C-based firmware development 
• Strong understanding of common embedded communication protocols including USB, I²C, SPI, UART, and BLE 
• Experience performing electrical analysis and simulation, including signal integrity, power integrity, and noise mitigation in compact electronic systems 
• Demonstrated experience delivering hardware–software integrated products from early concept through verification, validation, and commercialization 
• Experience working within regulated development environments, including familiarity with FDA design controls, design history files (DHF), and traceable engineering documentation 
• Exceptional hands-on engineering capability, with a proven ability to troubleshoot complex electrical and system-level issues 
• Ability to produce clear, rigorous engineering documentation including design analysis, test reports, verification protocols, and design rationale 
• Strong communication and collaboration skills across multidisciplinary teams including firmware, mechanical engineering, product management, clinical, and manufacturing teams 
• Ability to communicate complex technical concepts clearly to both engineering peers and executive leadership 

Preferred Qualifications: 

• M.S. in Electrical Engineering or a related technical field 
• Experience developing wearable medical devices or compact battery-powered consumer electronics 
• Experience designing low-power embedded systems for continuous or wearable operation 
• Experience working within medical device quality systems and regulated product development processes (e.g., FDA design controls, ISO 13485) 
• Demonstrated success leading complex hardware programs from early development through commercialization 
• Experience collaborating with contract manufacturers and external development partners during product development and manufacturing scale-up
• Experience designing for and supporting EMC/EMI compliance and testing, including familiarity with IEC 60601, EN 61326, or comparable standards 

Compensation: 

• Base pay: $140,000–$170,000 per year + bonus

Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers is dedicated to delivering prescription-grade therapy with an outstanding user experience. We have pioneered the world’s first drug-free wearable therapy, clinically proven to alleviate symptoms in adults with drug-resistant Restless Legs Syndrome (RLS). Be part of our mission to transform healthcare, improve lives, and drive meaningful change with Noctrix Health. 

Noctrix Health is seeking a high-caliber Senior Manufacturing & Supply Chain Engineer to drive our global manufacturing and domestic fulfillment strategy. This is an end-to-end "Cradle-to-Grave" operations role. You will manage our primary suppliers in Asia and secondary partners in the USA, lead technical validations (IQ/OQ/PQ) at supplier sites, and oversee our domestic DME (Durable Medical Equipment) fulfillment and RMA operations. The successful candidate will be a technical operator who can bridge the gap between engineering rigor and supply chain agility. This position reports to the VP of Supply Chain & Operations.  

**This is a full-time, in-person role based in Pleasanton, CA.** 

Responsibilities: 

• Serve as the primary lead for Asia-based and USA-based contract manufacturers, managing supplier performance, costs, production schedules, and strategic partnerships 
• Lead and perform IQ, OQ, and PQ validations at supplier facilities to ensure manufacturing lines meet Noctrix quality and compliance standards 
• Collaborate with supplier engineers to optimize manufacturing processes, reduce scrap rates, and improve overall yield 
• Travel internationally (primarily Asia) to conduct supplier audits, oversee production launches, and resolve technical issues on-site 
• Analyze supplier capacity against sales forecasts to identify bottlenecks and lead long-term manufacturing scale-up planning 
• Develop and manage global supply and demand models to balance international lead times with domestic demand fluctuations 
• Execute strategic sourcing and procurement for components and finished goods 
• Direct daily DME operations to ensure accurate, compliant order fulfillment 
• Manage and supervise DME technicians, setting priorities for fulfillment and technical work 
• Design and implement custom tools (automation scripts, advanced trackers, ERP enhancements) to improve operational efficiency and fulfillment throughput 
• Own the RMA process, performing physical investigations of returned medical devices to identify root causes and failure modes 
• Provide closed-loop feedback to supplier engineers and internal R&D teams to drive continuous product and process improvement 

Requirements: 

• 7+ years in Supply Chain or Operations within the Medical Device (ISO 13485/FDA) industry 
• Hands-on experience with IQ/OQ/PQ and manufacturing process validation 
• Proven experience managing Asia-based contract manufacturers and navigating global logistics 
• Experience in a DME environment using order fulfillment and shipping tools. 
• Strong ability to build/enhance tools (Advanced Excel/VBA, SQL, or Low-code platforms) to automate workflows 
• Bachelor’s degree in Engineering (Mechanical, Industrial, or Electrical) or a related technical field is strongly preferred 
• Must be able to work at the office at least three days a week 

Preferred: 

• Deep understanding of DMEPOS quality standards. 
• Experience in Lean Manufacturing or Six Sigma (Green/Black Belt)
• Ability to troubleshoot hardware and perform root-cause analysis

Compensation: 

• Base pay: $125,000–$150,000 per year + bonus