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Medical Device Development Jobs in Houston, TX (NOW HIRING)

USA Firmware

Principal Embedded Firmware Engineer

Houston, TX · On-site

$98K - $134K/yr

... development, verification, and maintenance of advanced safety-critical medical device firmware. This role focuses on Class I, II, and III medical devices, including neuromodulation platforms ...

USA Firmware

Principal Embedded Firmware Engineer

Houston, TX · On-site

$98K - $134K/yr

... development, verification, and maintenance of advanced safety-critical medical device firmware. This role focuses on Class I, II, and III medical devices, including neuromodulation platforms ...

Viant

Commercial Development Manager

Houston, TX · On-site

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

medplast

Commercial Development Manager

Houston, TX · On-site

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

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All JobsMedical Device Development JobsMedical Device Development Jobs in Houston, TX

Medical Device Development information

See Houston, TX salary details

$27.7K

$51K

$77.4K

How much do medical device development jobs pay per year?

As of Aug 21, 2026, the average yearly pay for medical device development in Houston, TX is $51,012.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,600.00 and $57,300.00 per year, depending on experience, location, and employer.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.

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

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

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

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

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

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What cities near Houston, TX are hiring for Medical Device Development jobs?

Cities near Houston, TX with the most Medical Device Development job openings:

Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in Houston, TX as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $51,012 per year, or $24.5 per hour.

Principal Embedded Firmware Engineer

USA Firmware

Houston, TX

$98K - $134K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted yesterday

Job description

A Houston-based professional engineering firm is seeking a Principal Embedded Firmware Engineer to lead the architecture, design, development, verification, and maintenance of advanced safety-critical medical device firmware. This role focuses on Class I, II, and III medical devices, including neuromodulation platforms, implantable pulse generators, and artificial pancreas systems. The position requires leadership in embedded firmware development, risk and reliability analysis, secure design, wireless communication systems, and low-power embedded architectures.

The Principal Embedded Firmware Engineer will collaborate with multidisciplinary engineering teams across software, electrical, and mechanical disciplines to deliver high-quality products on schedule. The role also includes mentoring engineers, leading project execution strategy, driving technical innovation, and serving as a customer-facing technical leader.

Key responsibilities include:

  • Firmware architecture, coding, testing, integration, and verification
  • Safety-critical embedded systems development
  • Low-power embedded design and optimization
  • Development of wireless and wired communication interfaces (BLE, UART, I2C, USB, NFC)
  • Cybersecurity implementation and FOTA update strategies
  • Risk assessment, technical planning, and lifecycle management
  • Cross-functional collaboration and technical mentorship

Candidates should have extensive experience with C/C++, Python, ARM Cortex architectures, RTOS and bare-metal systems, medical device development processes, and relevant regulatory standards such as IEC 62304 and ISO 14971.

Requirements

  • MS degree in a relevant engineering or technical field, or equivalent experience
  • 15+ years of experience in embedded firmware or related specialized engineering fields
  • Minimum 10 years of experience working within a requirements-driven structured development process
  • Strong experience with embedded microcontrollers, bare-metal systems, and RTOS environments
  • Proficiency in C/C++, Python, and assembly language programming
  • Experience with ARM Cortex architectures and low-power embedded system design
  • Experience with communication interfaces including UART, I2C, USB, BLE, and NFC
  • Knowledge of cybersecurity principles and firmware-over-the-air (FOTA) updates
  • Experience with firmware architecture, device drivers, testing, integration, and verification
  • Familiarity with software development tools such as Jira, Git, GitHub, and BitBucket
  • Working knowledge of IEC 62304, ISO 13485, ISO 14971, and other relevant medical device standards
  • Experience with safety-critical applications and medical devices preferred
  • Strong troubleshooting, root-cause analysis, and risk assessment skills
  • Excellent communication, leadership, collaboration, and mentoring abilities
  • Proven ability to lead projects through the full software development lifecycle from architecture through release and maintenance

Benefits

Company-paid Vision and Dental insurance

Discounted Medical insurance

401(k) matching program

Opportunity to work on cutting-edge medical device technologies

Collaborative, multidisciplinary engineering environment

Exposure to a wide variety of advanced medical device projects

Continuous learning and professional growth opportunities

Leadership and mentorship opportunities within technical teams

High-impact work focused on improving patient outcomes and quality of life

Apply