Principal Software Quality Engineer, SaMD, Cybersecurity

Job not on LinkedIn

🕒 6 days ago

🇺🇸 United States – Remote

💵 $161k - $196k / year

⏰ Full Time

🔴 Lead

🔧 QA Engineer (Quality Assurance)

👻 Ghost score 0%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

AirStrip

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2006

🏥 Healthcare

☁️ SaaS

💰 $50M Debt Financing - Airstrip Technologies on 2025-10

Healthcare • SaaS

AirStrip is a vendor-agnostic clinical surveillance and patient-monitoring platform that aggregates real-time waveforms, ECGs, alarms, and other clinical data from monitors, EMRs and medical devices and delivers them to clinicians via mobile and web applications. AirStrip’s products include solutions for patient monitoring, obstetrics (maternal/fetal monitoring), cardiology (12-lead ECGs, STEMI notifications), alarm management and analytics, telemetry optimization, and decision support. The platform emphasizes near-real-time waveform access, alarm triage/dispatch, diagnostic-quality ECG capture and secure EHR transmission, and meets industry security and HIPAA requirements.

📋 Description

• Provide independent quality oversight of software development activities, ensuring compliance with SDLC procedures, design controls, and applicable regulatory requirements • Review and approve software development plans, requirements, architecture and design documentation, verification and validation protocols, test reports, and release documentation • Ensure requirements traceability, configuration management, software risk management, and design controls throughout the product lifecycle • Evaluate software changes for impacts on patient safety, product effectiveness, cybersecurity, and regulatory submission requirements • Integrate risk-based quality controls into Agile development, DevSecOps, CI/CD pipelines, and automated testing processes • Oversee medical device cybersecurity activities, including threat modeling, security risk assessments, vulnerability analyses, and verification of cybersecurity risk controls • Ensure compliance with FDA cybersecurity requirements, IEC 81001-5-1, AAMI TIR57, AAMI TIR97, and other relevant standards • Oversee Software Bills of Materials (SBOMs), third-party software components, vulnerability monitoring, patch management, and cybersecurity incident response • Review cybersecurity testing evidence, including penetration testing, static and dynamic application security testing, and software composition analysis • Oversee software verification and validation, including unit, integration, system, regression, performance, and security testing • Support software and cybersecurity documentation for FDA 510(k) submissions, international regulatory filings, audits, and inspections • Ensure completeness, accuracy, and traceability of software Design History Files, risk management documentation, and QMS records • Lead or support nonconformance investigations, root cause analysis, CAPA, and evaluation of complaints, defects, and postmarket cybersecurity vulnerabilities • Establish and monitor software quality metrics, including defect trends, test coverage, CAPA effectiveness, cybersecurity remediation, and release quality • Serve as a software quality and cybersecurity subject matter expert, communicate risks and compliance status to management, and drive continuous improvement

🎯 Requirements

• Bachelor’s degree in Software Engineering, Computer Science, Biomedical Engineering, Electrical Engineering, Cybersecurity, or a related technical discipline • Minimum of 8 years of experience in software quality engineering, software development, software verification and validation, or related disciplines • Minimum of 5 years of experience working with FDA-regulated medical devices, Software as a Medical Device (SaMD), digital health, or connected medical device software • Demonstrated experience with IEC 62304, ISO 13485, ISO 14971, FDA design controls, and software risk management • Experience with medical device cybersecurity, secure software development, cybersecurity risk assessments, and vulnerability management • Experience with Agile software development, DevSecOps, CI/CD pipelines, automated testing, and software configuration management • Experience supporting FDA regulatory submissions, software change assessments, audits, CAPA investigations, and regulatory inspections • Experience with cloud-based software, healthcare applications, or connected medical device systems preferred • Advanced degree or relevant professional certifications, such as CISSP, CSSLP, CISM, ASQ CSQE, CQE, or applicable auditor certifications, preferred • Advanced knowledge of medical device software quality engineering, software development lifecycle processes, design controls, and applicable FDA and international regulatory requirements • Strong understanding of medical device cybersecurity standards, secure software development practices, and cybersecurity risk management • Proficiency in software verification and validation, automated testing, requirements traceability, and configuration management • Working knowledge of Jira, Azure DevOps, GitHub, and GitLab • Understanding of cloud-based architectures, APIs, network security, third-party software, and healthcare interoperability technologies • Strong analytical, critical thinking, problem-solving, and risk-based decision-making skills • Demonstrated ability to provide technical leadership and influence cross-functional teams without direct reporting authority • Ability to balance regulatory compliance, patient safety, cybersecurity considerations, and business objectives • Excellent written and verbal communication skills, including the ability to communicate complex technical and regulatory information to diverse audiences • Strong organizational skills with the ability to manage multiple priorities in a fast-paced software development environment • Detail-oriented, proactive, and accountable, with a commitment to continuous improvement, quality ownership, and sound professional judgment

🏖️ Benefits

• Robust medical, dental, and vision insurance • Financial planning assistance • Physical and mental wellness discounts • Unlimited access to online learning platform • Paid Time Off (hourly) / Flex Time Off (salaried) programs for Full Time employees • Growth and Development opportunities • 401(k), including a 3% company match • Paid Holidays • Paid Parental Leave, including a flexible return-to-work program • Employee Assistance Program • Discounts on popular cell phone plan providers • Life & Disability Insurance

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume