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Medical Device Engineer Jobs in Texas (NOW HIRING)

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 ...

Frisco, TX (Onsite) We need engineers who have experience in design & development and testing. But ... a highly safety critical handheld medical device. Understand the GUI design developed in C ...

Design Quality Engineer, SaMD

Austin, TX ยท On-site

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

Design Quality Engineer, SaMD

Austin, TX ยท On-site

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

Quality Engineer

El Paso, TX ยท On-site

$34 - $35/hr

Title: Engr 1, Quality Client ... Medical Device Manufacturing domain Location: El Paso, TX 79912 Duration: 12 months (Possibility of ...

Senior Process Engineer

Stafford, TX ยท On-site

$90K - $117K/yr

The Senior Process Engineer is a key individual contributor responsible for the development ... supporting medical device products. This role partners cross-functionally with Quality ...

Senior Process Engineer

Stafford, TX

$90K - $117K/yr

The Senior Process Engineer is a key individual contributor responsible for the development, optimization, validation, and sustainment of manufacturing processes supporting medical device products.

... medical device software lifecycle. * Learn and apply best practices for LDT software and create and manage all applicable documentation. * Participate in risk assessments for software products ...

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

Showing results 41-60

Medical Device Engineer information

See Texas salary details

$19

$46

$90

How much do medical device engineer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for medical device engineer in Texas is $46.43, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $55.53 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device engineer, and why are they important?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What does a medical device engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What are some common challenges medical device engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

What does a medical device engineer do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

What are the most commonly searched types of Medical Device Engineer jobs in Texas? The most popular types of Medical Device Engineer jobs in Texas are:
What cities in Texas are hiring for Medical Device Engineer jobs? Cities in Texas with the most Medical Device Engineer job openings:
Infographic showing various Medical Device Engineer job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $96,577 per year, or $46.4 per hour.

Cybersecurity Engineer

Spectral MD Inc

Dallas, TX โ€ข On-site

Full-time

Re-posted 29 days ago


Job description

Position Summary:

Spectral AI, Inc. (Spectral) is seeking a Cybersecurity Engineer to join our growing design and development team. The position is based in Dallas, Texas, with hybrid work flexibility in accordance with the Spectral Employee Handbook guidelines. 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 regulations, international standards (e.g.. ANSI/AAMI SW 96:2003, IEC 62304, IEC 81001, ISO 14971, ISO 27001), and organizational security policies. The engineer will collaborate closely with Software Engineering, Hardware Engineering, Quality Assurance, Regulatory Affairs, Biomedical Engineering, Data Science, Systems Engineering, and IT internal teams to embed cybersecurity into design controls, risk management, regulatory submissions, and post-market surveillance activities.

Essential Duties and Responsibilities:

Product Cybersecurity

  • Institute Security-by-Design practices throughout the entire lifecycle of the Spectral device software, AI models, firmware, and hardware.
  • Develop and maintain cybersecurity standard operating procedures (SOPs) and work instructions that support compliance with regulatory and security requirements in all target markets for Spectral products.
  • Support design reviews by providing security input and ensuring cybersecurity is integrated into design controls.

Cybersecurity Risk Management

  • Perform cybersecurity risk assessments for medical device systems using structured methodologies (Threat Modeling, STRIDE, DREAD, Attack Trees, SBOM analysis).
  • Execute and document risk evaluation aligned with AAMI TIR57, AAMI TIR97, FDA Premarket Cybersecurity Guidance, and ISO 14971.
  • Participate actively in Coordinated Vulnerability Disclosure (CVD) processes, working with internal team and vendors to ensure vulnerabilities are responsibly reported, remediated, and communicated in alignment with industry best practices.
  • Maintain and periodically update cybersecurity documentation and supporting artifacts, including:
    • Security risk assessment
    • Security risk management reports
    • Threat models
    • Cybersecurity requirements, testing, and traceability matrices in alignment with FDA guidance and IEC 81001

Secure Software Development (IEC 81001 and IEC 62304)

  • Collaborate with software engineers to implement secure coding practices and structured code review processes.
  • Ensure correct implementation of security requirements, encryption standards, authentication and authorization controls, and security-relevant logging.
  • Evaluate SOUP/OTS components for vulnerabilities, maintenance status, and compliance with FDA software bill of material (SBOM) requirements.
  • Support the creation and ongoing maintenance of SBOM (e.g. CycloneDX, SPDX) using automated tools such as HELM and Dependency-Check.

Vulnerability and Patch Management

  • Perform vulnerability scanning across firmware, software, cloud services, Linux-based, and Windows-based cart devices.
  • Triage and validate Common Vulnerabilities and Exposures (CVEs) relevant to device components, run-time environments, and third-party libraries.
  • Prepare vulnerability mitigation plans and support development teams during remediation.
  • Support integration of security controls across local, handheld, and cloud-connected medical devices.

Penetration Testing and Verification Support

  • Prepare documentation, architecture diagrams, and accounts for test execution.
  • Track findings, analyze root causes, and support remediation verification.

Incident Response and Monitoring

  • Assist in establishing cybersecurity monitoring processes for fielded devices and cloud environments.
  • Investigate security anomalies and incidents, perform log analysis, and support corrective/preventive actions (CAPA).

Qualifications:

Required education and experience:

  • Bachelor’s degree or above in Computer Science, Cybersecurity, Electrical/Computer Engineering, or a related field.
  • 3–5 years of proven experience in cybersecurity engineering, ideally within medical devices, healthcare technology, regulated software, or other safety-critical systems.
  • Demonstrated proficiency in technical writing, ensuring accurate, comprehensive, and well‑structured documentation for software cybersecurity.

Knowledge, Skills and Abilities:

  • FDA Premarket Cybersecurity Guidance
  • IEC 62304 Software Lifecycle
  • AAMI TIR57 / TIR97
  • OWASP Top 10, CWE, and secure coding principles
  • Familiarity with Transport Layer Security (TLS), certificate management, encryption protocols (e.g. AES, RSA), and authentication/authorization models.
  • Understanding of cybersecurity vulnerabilities and FDA reporting requirements
  • Understanding of Windows and Linux OS hardening, cloud security (AWS/Azure), and secure configuration.

Preferred Qualifications

  • Experience supporting FDA medical device submissions with cybersecurity documentation.
  • Hands-on experience with medical cart or handheld device security (Windows, Linux, embedded OS).
  • Experience with cloud-connected medical systems (AWS IoT, secure APIs, VPN connections).
  • Certifications such as Security+, CySA+, CISSP, GSEC, CEH, or industry equivalent.

Soft Skills

  • Excellent written and verbal communication skills in English.
  • Detail-oriented, strong analytical and problem-solving skills.
  • Ability to prepare quality cybersecurity documentation suitable for regulatory review.
  • Ability to collaborate across functional teams such as engineering, QA/RA, hardware, and clinical teams.
  • Comfortable managing multiple concurrent security tasks.

Physical Requirements:

  • Prolonged periods of sitting at a desk and working on a computer.

Travel:

Occasional support during off-hours for security events or release deadlines

Equal Employment Opportunity:

Spectral AI, Inc. is an equal opportunity and affirmative action employer. All applicants will be considered for employment without regard to race, color, ancestry, national origin, sex, gender, sexual orientation, marital status, religion, age, disability, gender identity, results of genetic testing, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws.