Echo Neurotechnologies

The Hardware Test Engineer will be responsible for testing custom Echo hardware devices and subsystems. This includes executing in-house design verification tests and collaborating with the engineering team to develop custom tests. | Candidates must have a bachelor's degree in a relevant engineering field and a minimum of 5 years of industry experience in testing electro-mechanical hardware devices. Experience with verification testing and quality systems is also required. | Company Overview Echo Neurotechnologies is an exciting new startup in the Brain-Computer Interface (BCI) space, driving innovation through advanced hardware engineering and AI solutions. Our mission is to deliver cutting-edge technologies that restore autonomy to people living with disabilities and improve their quality of life. Team Culture Join a small, dedicated team of knowledgeable and motivated professionals. Our early-stage environment offers the opportunity to take ownership of broad decisions with significant and long-lasting impact. We emphasize continuous learning and growth, fostering cross-functional collaboration where your contributions are vital to our success. Role Overview We are seeking an experienced Hardware Test Engineer to verify the Echo hardware system. The candidate will be responsible for testing custom Echo hardware devices and subsystems. The candidate will also drive development and bring-up of custom test systems. Primary Role and Responsibilities Execute in-house design verification tests Execute testing with external test labs Work with engineering team to develop custom tests Collaborate with design engineers to characterize custom hardware Dry-running tests for transfer to vendors Qualifications Bachelor's degree in Mechanical Engineering, Electrical Engineering, Chemical Engineering, or related field Minimum 5 years of industry experience in testing electro-mechanical hardware devices Experience with executing verification testing and participating in the test design loop Experience with writing test protocols and documenting results in formal test reports Experience working within a quality system Other Qualifications Master’s degree in Mechanical Engineering, Electrical Engineering, Chemical Engineering, or a related field Familiarity with medical device compliance and standards Strong collaboration mindset Superior written and verbal communication skills Exceptional organizational skills and attention to detail Occasional travel to vendors (<10%) What We Offer An opportunity to work on exciting, cutting-edge projects to transform patients’ lives in a highly collaborative work environment. Competitive compensation, including stock options. Comprehensive benefits package. 401(k) program with matching contributions. Equal Opportunity Employer Echo Neurotechnologies is an Equal Opportunity Employer (EOE). We celebrate diversity and are committed to creating an inclusive environment for all employees. Confidentiality All applications will be treated confidentially. Applicants may be asked to sign an NDA after the initial stages of the interview process.

Lead quality assurance activities across product development lifecycle ensuring compliance with medical device regulations and standards. | 8+ years quality engineering experience in medical device development, strong knowledge of FDA and ISO standards, hands-on risk management, and excellent documentation skills. | Company Overview Echo Neurotechnologies is an exciting new startup in the Brain-Computer Interface (BCI) space, driving innovation through advanced hardware engineering and AI solutions. Our mission is to deliver cutting-edge technologies that restore autonomy to people living with disabilities and improve their quality of life. Team Culture Join a small, dedicated team of knowledgeable and motivated professionals. Our early-stage environment offers the opportunity to take ownership of broad decisions with significant and long-lasting impact. We emphasize continuous learning and growth, fostering cross-functional collaboration where your contributions are vital to our success. As a Sr. Quality Engineer, you will work with the cross-functional team to act as a champion of Design Quality Assurance and Engineering activities throughout the product development lifecycle. You hold your work and teams to the highest quality standards and ensure all applicable compliance standards and regulations are met. This is a hands-on role supporting multiple domains across hardware and software engineering, supplier quality and quality system implementation. Primary Duties & Responsibilities: Participate in ongoing implementation of the Quality Management System (QMS) in conformance with US FDA Quality System Regulations, ISO 13485, IEC 62304, IEC 60601 and IEC 62366-1 and other relevant standards Support the product development team in creation of design history files (DHFs) including product requirements, software and hardware design specifications, design verification and validation test protocols and reports, risk management file, cybersecurity risk files, biocompatibility and sterilization validation deliverables, traceability matrices, etc. Guide and lead risk management activities, including failure modes and effects analysis (FMEA) and hazards analysis, in alignment with ISO 14971 Engage and collaborate with suppliers and support design, development and design transfer activities Support and participate in internal and external audits, coordinating and providing documentation and evidence of compliance Support root cause analysis for nonconformances, defects and CAPAs, issue management, management review and quality data analysis Foster a collaborative environment, champion continuous improvement initiatives and promote a quality culture across the organization Qualifications: Bachelor’s or Master’s degree in Engineering (e.g., Biomedical, Mechanical, Electrical, or related field). 8+ years of quality engineering or in medical device development from concept development to production release. Strong understanding of medical device regulations and standards (FDA, ISO 13485, IEC 62304, ISO 14971, IEC 62366-1, IEC 60601) and experience working in a regulated environment Experience with software and hardware V&V activities, experience with AI/ML technology is a plus Hands-on experience with risk management tools (e.g. FMEA, risk analysis) and design controls Experience in establishing work relationships across multi-disciplinary teams and with partners in different time zones, building trust and demonstrating critical thinking Experience in navigating ambiguity, bringing clarity to complex situations and thriving in a fast-paced environment Skills and Abilities: Proficient in working in eQMS tools with impeccable documentation skills Superior written and verbal communication skills to interface with cross-functional teams and regulatory bodies Strong analytical skills and excellent problem-solving skills Exceptional organizational skills and attention to detail What We Offer An opportunity to work on exciting, cutting-edge projects to transform patients’ lives in a highly collaborative work environment. Competitive compensation, including stock options. Comprehensive benefits package. 401(k) program with matching contributions. Equal Opportunity Employer Echo Neurotechnologies is an Equal Opportunity Employer (EOE). We celebrate diversity and are committed to creating an inclusive environment for all employees. Confidentiality All applications will be treated confidentially. Applicants may be asked to sign an NDA after the initial stages of the interview process.