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Medical Device Cybersecurity Jobs in Texas (NOW HIRING)

Spectral MD Inc

Cybersecurity Engineer

Dallas, TX · On-site

The Cyber Security Engineer will support the design, development, and maintenance of secure medical device software systems, ensuring that cybersecurity controls are resilient and compliant with FDA ...

USA Firmware

Principal Embedded Firmware Engineer

Houston, TX · On-site

$98K - $134K/yr

... medical device firmware. This role focuses on Class I, II, and III medical devices, including ... Cybersecurity implementation and FOTA update strategies * Risk assessment, technical planning, and ...

USA Firmware

Principal Embedded Firmware Engineer

Houston, TX · On-site

$98K - $134K/yr

... medical device firmware. This role focuses on Class I, II, and III medical devices, including ... Cybersecurity implementation and FOTA update strategies * Risk assessment, technical planning, and ...

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

AI/ML-enabled medical-device experience. * Familiarity with IMDRF GMLP principles. * Cybersecurity documentation experience for medical devices. * Usability / human factors engineering experience.

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

AI/ML-enabled medical-device experience. * Familiarity with IMDRF GMLP principles. * Cybersecurity documentation experience for medical devices. * Usability / human factors engineering experience.

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

AI/ML-enabled medical-device experience. * Familiarity with IMDRF GMLP principles. * Cybersecurity documentation experience for medical devices. * Usability / human factors engineering experience.

Vytwo

Bioinformatics Pipeline Test Engineer

Prosper, TX · On-site

... details doc) for medical device software lifecycle. * Learn and apply best practices for LDT ... Familiarity with software related Cybersecurity risk management such as FDA Cybersecurity guidance ...

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Medical Device Cybersecurity information

What are some common challenges faced by professionals in medical device cybersecurity, and how can they be addressed?

Professionals in medical device cybersecurity often encounter challenges such as integrating security measures into legacy devices, ensuring compliance with evolving regulations, and balancing usability with robust protection. Collaborative efforts with engineering, regulatory, and clinical teams are crucial to embedding security throughout the product lifecycle. Staying current with threat intelligence and participating in cross-functional risk assessments also help anticipate and address vulnerabilities proactively.

What is medical device cybersecurity?

Medical device cybersecurity refers to the protection of medical devices and the data they process from cyber threats and unauthorized access. As medical devices become increasingly connected to hospital networks and the internet, robust cybersecurity measures are essential to ensure patient safety and protect sensitive health information. This field involves identifying vulnerabilities, implementing safeguards, and complying with regulatory requirements to reduce the risk of cyberattacks on medical technology.

What is the difference between Medical Device Cybersecurity vs Medical Device Quality Assurance?

AspectMedical Device CybersecurityMedical Device Quality Assurance
Required CredentialsCertifications in cybersecurity, such as CISSP or CISA; knowledge of medical device regulationsCertifications in quality management, like CQE or ISO 13485 auditor
Work EnvironmentIT security teams, R&D, regulatory compliance in healthcare settingsManufacturing, clinical, and regulatory environments focused on product quality
Employer & Industry UsageMedical device manufacturers, healthcare providers, cybersecurity firmsMedical device companies, regulatory agencies, quality assurance firms

Medical Device Cybersecurity focuses on protecting medical devices from cyber threats, ensuring data integrity and security. Medical Device Quality Assurance emphasizes maintaining product quality, safety, and compliance throughout development and manufacturing. While both roles support patient safety, cybersecurity specialists address digital vulnerabilities, whereas quality assurance professionals ensure the device meets regulatory standards.

What are the key skills and qualifications needed to thrive in medical device cybersecurity, and why are they important?

To thrive in Medical Device Cybersecurity, you need a solid background in cybersecurity principles, risk management, and biomedical engineering, often supported by a relevant degree and certifications like CISSP or CISM. Familiarity with regulatory standards (such as FDA cybersecurity guidelines), network security tools, and vulnerability assessment systems is essential. Strong analytical thinking, attention to detail, and effective communication skills help professionals collaborate with cross-functional teams and address complex security challenges. These skills are crucial to ensure medical devices remain secure from cyber threats, protecting patient safety and maintaining regulatory compliance.
What are popular job titles related to Medical Device Cybersecurity jobs in Texas? For Medical Device Cybersecurity jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Medical Device Cybersecurity jobs in Texas look for? The top searched job categories for Medical Device Cybersecurity jobs in Texas are:
What cities in Texas are hiring for Medical Device Cybersecurity jobs? Cities in Texas with the most Medical Device Cybersecurity job openings:
Medical Device Cybersecurity jobs near you
Infographic showing various Medical Device Cybersecurity job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Senior Quality Engineer, Cybersecurity

Verily Life Sciences

Dallas, TX • On-site

$87K - $118K/yr

Full-time

Posted 22 days ago

Job description

Who We Are
Verily Health is a data platform and technology company purpose-built to power AI-enabled precision health solutions that accelerate research and improve care for individuals and communities. Uniquely positioned at the intersection of technology, data science, and healthcare, Verily transforms multimodal health data into insights, models, and actions that make healthcare more personalized, predictive, and precise.
Description
The Senior Quality Engineer, Cybersecurity is a hands-on individual contributor and subject matter expert who bridges quality engineering and cybersecurity across Verily's consumer, research, and medical device (SaMD) product portfolio. This role champions quality and security throughout the software development lifecycle - partnering closely with engineering, security, and product teams to ensure that cybersecurity processes are embedded in the QMS, meet applicable regulatory requirements, and scale across Verily's evolving product domains. The role proactively identifies risk, drives cross-functional initiatives, and brings deep technical fluency in both quality engineering and cybersecurity to protect the integrity of Verily's systems, data, and regulated products.
Responsibilities
  • Leads ongoing implementation and continuous improvement of the Software Quality Management System (QMS) across consumer, research, and SaMD product domains - in conformance with FDA QMSR, ISO 13485:2016 design controls, and SDLC processes - integrating internal best practices and medical device industry standards. Serves as the Quality Lead for the cybersecurity process, partnering closely with the Security team to embed security requirements, threat modeling, vulnerability management, and secure coding practices into the SDLC and QMS in alignment with FDA cybersecurity guidance and AAMI TIR57.
  • Guides software development teams in the creation and maintenance of Design and Development Files (DDFs), including software development plans, verification and validation plans, software requirements specifications, architecture and design documents, design and code reviews, Risk Management Files (RMF), test protocols and reports, and traceability matrices.
  • Supports integration of ISO 14971 risk management, IEC 62366 usability engineering, and FDA cybersecurity guidance into SDLC processes, ensuring a cohesive and compliant approach to product safety, security, and usability across the development lifecycle.
  • Supports post-market cybersecurity surveillance activities for SaMD and LLM-enabled products, including monitoring for emerging threats, coordinating vulnerability disclosures, and assessing the impact of security findings on regulated product safety and performance.
  • Provides CAPA, complaints, audit, and QMS support related to software and cybersecurity incidents, driving root cause analysis and effective corrective actions across product teams.

Qualifications
Minimum Qualifications
  • Bachelor's degree in Computer Science, Software Engineering, Informatics, Biomedical Engineering, or a related technical field; or equivalent practical experience with 5+ years in software quality engineering within the FDA QMSR / ISO 13485 medical device industry, with primary focus on Software as a Medical Device (SaMD).
  • Proven expertise in medical device cybersecurity, including working knowledge of FDA premarket and postmarket cybersecurity guidance and applicable standards (e.g., AAMI TIR57).
  • Demonstrated experience applying IEC 62304 (Medical Device Software Lifecycle Processes), ISO 14971 (Risk Management), IEC 62366 (Usability Engineering), and AAMI TIR57 within a regulated software development environment.
  • Experience collaborating directly with software development and security teams, with proficiency in Google Workspace, Jira, GitHub, and document control systems to operationalize quality and cybersecurity requirements within engineering workflows.

Preferred Qualifications
  • Experience with AI/ML-enabled medical device products, including familiarity with FDA AI/ML SaMD guidance, predetermined change control plans (PCCP), and post-market performance monitoring for generative AI applications; experience using generative AI tools (e.g., Gemini, Claude, ChatGPT) to enhance quality and compliance workflows is a plus.
  • Experience with digital health, Health IT, mobile medical applications, or consumer health products, with working knowledge of scalable QMS and SDLC approaches across wellness, low-risk, and high-risk software classifications.
  • Demonstrated ability to implement and continuously improve Software QMS and secure SDLC processes using agile/scrum methodologies, best-practice tooling, and iterative development frameworks in a fast-paced, innovative environment.
  • Relevant cybersecurity certification (e.g., AAMI Cybersecurity Certificate, CISSP, or equivalent) and/or quality certification (e.g., ASQ CQE); or advanced degree in a related technical or biomedical field.
  • Excellent cross-functional communication, organizational, and leadership skills, with a proven ability to drive quality and cybersecurity initiatives with minimal supervision across engineering, security, and product teams.

Qualified applicants must not require employer sponsored work authorization now or in the future for employment in the United States.
The US base salary range for this full-time position is $113,000 - $170,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.
Verily Health Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you'd like more information on your EEO rights under the law, please click here.
If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.

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