{"schemaVersion":"jobsearcher.job.v1","id":"ff7eb09f6c7f579fb8d62a1a","url":"https://jobsearcher.com/jobs/ff7eb09f6c7f579fb8d62a1a","canonicalUrl":"https://jobsearcher.com/jobs/ff7eb09f6c7f579fb8d62a1a","title":"Systems Engineer II","description":"ATEC is seeking a Systems Engineer II to support the design, development, and integration of next‑generation neuromonitoring, navigation, imaging, and cloud‑connected surgical platforms.\n\nThis role contributes across the full product lifecycle—from refining user needs and authoring requirements through technical execution, verification/validation, design transfer, and post‑market investigations—while collaborating closely with mechanical, electrical, software, quality, regulatory, marketing, and operations teams.\n\nThe systems developed in this role directly support surgeons in improving surgical accuracy, efficiency, and patient safety in spine surgery.\n\nEssential Duties and Responsibilities\n\nSystems Engineering Leadership\n\nSupportthe development, decomposition, and management of system and subsystem requirements, consistent with INCOSE‑aligned best practices.\n\nSupportsystem architecture, interfaces, and integration strategies for multi‑disciplinary systems spanning software, hardware, and mechanical components.\n\nPerform risk analyses, hazard assessments, and support design control activities for regulated medical devices,ensuring system‑level safety mitigations that protect patients and clinical users.\n\nMaintain and update Design History File (DHF) documentation and support Change Order activities,supporting traceability and compliance required to safely deliver products into clinical use.\n\nCross‑Functional Collaboration\n\nPartner with marketing, clinical, software, hardware, mechanical, test, and quality/regulatory teams to refine user needs,translating surgeon and clinical feedback into system requirements that improve real‑world surgical workflows.\n\nSupportcross‑functional design reviews and provide analytical decision support through modeling, simulation, and system‑level analysis.\n\nCollaborate with Quality and Regulatory to ensure requirements traceability, verification strategy alignment, and submission‑ready documentation (e.g., 510(k) inputs).\n\nProject & Technical Leadership\n\nSupportkey engineering efforts, ensuring alignment with program timelines, risk posture, and business objectives.\n\nMaintain a strong presence in day‑to‑day project execution—driving structure, clarity, and alignment across cross‑functional engineering teams.\n\nWork closely with a project manager, or directly manage projects as appropriate, to drive clear timelines that are executed on time and on budget.\n\nMedical Device / Spine Domain\n\nDevelop and manage system requirements for intraoperative imaging, surgical navigation, data analytics, and workflow optimization technologies,that support increased procedural accuracy, reduced variability, and improved surgical efficiency.\n\nSupport integration of informatics platforms with imaging systems, surgical instrumentation, and intraoperative sensors.\n\nEnsure system design incorporates key clinical and technical considerations including surgical ergonomics, accuracy, latency, safety, sterilization, cybersecurity, and overall reliability.\n\nThe requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.\n\nExperience in requirements development, architecture definition, risk management, and verification/validation planning.\n\nWorking knowledge ofsoftware development life cycle (SDLC).\n\nFamiliarity with medical device product development life cycles.\n\nStrong communication skills with the ability to lead technical discussions, author clear technical documentation, and present effectively to leadership.\n\nPreferred Qualifications\n\nBachelor’s degree in engineering or related technical discipline (advanced degree preferred).\n\nExperience with surgical technologies, spine implants, navigation systems, robotics, or intraoperative imaging systems.\n\nExperience in regulated product development—medical device preferred (ISO 13485, ISO 14971, IEC 60601, design controls).\n\nFamiliarity with MBSE, SysML, Cameo, or similar systems modeling tools.\n\nINCOSE ASEP/CSEP certification or equivalent.\n\nExperience supporting verification planning, requirements traceability, risk management files, and system‑level contributions to regulatory submissions (e.g., 510(k) documentation).\n\nEducation and Experience\n\nUndergraduate degree in an engineering discipline, graduate degree preferred.\n\n2-5 years of engineering experience, including1year working in Systems Engineering, Systems Architecture, or multi‑disciplinary product development roles.\n\nEqual Employment Opportunity & Other Disclosures\nATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws.\n\nFor roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID‑19 vaccine, as applicable).\n\nAt this time, ATEC Spine does not sponsor employment visas for this position. Candidates must be authorized to work in the United States without the need for current or future employer sponsorship.\n\nSalary Range\nAlphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $100,000-$110,000 Full-Time Annual Salary\n\n#J-18808-Ljbffr","company":"Internetwork Expert","rawCompany":"internetwork expert","city":"Carlsbad","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-06-17T03:38:08.066Z","occupations":[{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"15-1299.08","title":"Computer Systems Engineers/Architects","slug":"computer-systems-engineers-architects"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Systems Engineer II","description":"ATEC is seeking a Systems Engineer II to support the design, development, and integration of next‑generation neuromonitoring, navigation, imaging, and cloud‑connected surgical platforms.\n\nThis role contributes across the full product lifecycle—from refining user needs and authoring requirements through technical execution, verification/validation, design transfer, and post‑market investigations—while collaborating closely with mechanical, electrical, software, quality, regulatory, marketing, and operations teams.\n\nThe systems developed in this role directly support surgeons in improving surgical accuracy, efficiency, and patient safety in spine surgery.\n\nEssential Duties and Responsibilities\n\nSystems Engineering Leadership\n\nSupportthe development, decomposition, and management of system and subsystem requirements, consistent with INCOSE‑aligned best practices.\n\nSupportsystem architecture, interfaces, and integration strategies for multi‑disciplinary systems spanning software, hardware, and mechanical components.\n\nPerform risk analyses, hazard assessments, and support design control activities for regulated medical devices,ensuring system‑level safety mitigations that protect patients and clinical users.\n\nMaintain and update Design History File (DHF) documentation and support Change Order activities,supporting traceability and compliance required to safely deliver products into clinical use.\n\nCross‑Functional Collaboration\n\nPartner with marketing, clinical, software, hardware, mechanical, test, and quality/regulatory teams to refine user needs,translating surgeon and clinical feedback into system requirements that improve real‑world surgical workflows.\n\nSupportcross‑functional design reviews and provide analytical decision support through modeling, simulation, and system‑level analysis.\n\nCollaborate with Quality and Regulatory to ensure requirements traceability, verification strategy alignment, and submission‑ready documentation (e.g., 510(k) inputs).\n\nProject & Technical Leadership\n\nSupportkey engineering efforts, ensuring alignment with program timelines, risk posture, and business objectives.\n\nMaintain a strong presence in day‑to‑day project execution—driving structure, clarity, and alignment across cross‑functional engineering teams.\n\nWork closely with a project manager, or directly manage projects as appropriate, to drive clear timelines that are executed on time and on budget.\n\nMedical Device / Spine Domain\n\nDevelop and manage system requirements for intraoperative imaging, surgical navigation, data analytics, and workflow optimization technologies,that support increased procedural accuracy, reduced variability, and improved surgical efficiency.\n\nSupport integration of informatics platforms with imaging systems, surgical instrumentation, and intraoperative sensors.\n\nEnsure system design incorporates key clinical and technical considerations including surgical ergonomics, accuracy, latency, safety, sterilization, cybersecurity, and overall reliability.\n\nThe requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.\n\nExperience in requirements development, architecture definition, risk management, and verification/validation planning.\n\nWorking knowledge ofsoftware development life cycle (SDLC).\n\nFamiliarity with medical device product development life cycles.\n\nStrong communication skills with the ability to lead technical discussions, author clear technical documentation, and present effectively to leadership.\n\nPreferred Qualifications\n\nBachelor’s degree in engineering or related technical discipline (advanced degree preferred).\n\nExperience with surgical technologies, spine implants, navigation systems, robotics, or intraoperative imaging systems.\n\nExperience in regulated product development—medical device preferred (ISO 13485, ISO 14971, IEC 60601, design controls).\n\nFamiliarity with MBSE, SysML, Cameo, or similar systems modeling tools.\n\nINCOSE ASEP/CSEP certification or equivalent.\n\nExperience supporting verification planning, requirements traceability, risk management files, and system‑level contributions to regulatory submissions (e.g., 510(k) documentation).\n\nEducation and Experience\n\nUndergraduate degree in an engineering discipline, graduate degree preferred.\n\n2-5 years of engineering experience, including1year working in Systems Engineering, Systems Architecture, or multi‑disciplinary product development roles.\n\nEqual Employment Opportunity & Other Disclosures\nATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws.\n\nFor roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID‑19 vaccine, as applicable).\n\nAt this time, ATEC Spine does not sponsor employment visas for this position. Candidates must be authorized to work in the United States without the need for current or future employer sponsorship.\n\nSalary Range\nAlphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $100,000-$110,000 Full-Time Annual Salary\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T03:38:08.066Z","dateModified":"2026-06-17T03:38:08.066Z","hiringOrganization":{"@type":"Organization","name":"Internetwork Expert","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Carlsbad","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"ff7eb09f6c7f579fb8d62a1a"},"url":"https://jobsearcher.com/jobs/ff7eb09f6c7f579fb8d62a1a"}}