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Medical Device Integration Jobs in Texas (NOW HIRING)

Develop software integration test plan and protocols against design input docs & code for embedded handheld battery-operated medical device & execute them as per process defined for Medical device SW ...

Develop software integration test plan and protocols against design input docs & code for embedded handheld battery-operated medical device & execute them as per process defined for Medical device SW ...

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 ... Firmware architecture, coding, testing, integration, and verification * Safety-critical embedded ...

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 ... Firmware architecture, coding, testing, integration, and verification * Safety-critical embedded ...

Medical Orthopedic Rep

Beaumont, TX · On-site

$91K - $122K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Quality Engineer

Longview, TX

$64K - $82K/yr

Ensure integration of quality systems to ensure a common quality system throughout the facility and ... Ensure the quality management system meets the company's medical device expectations and goals.

Showing results 21-40

Medical Device Integration information

See Texas salary details

$12

$27

$51

How much do medical device integration jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for medical device integration in Texas is $27.80, according to ZipRecruiter salary data. Most workers in this role earn between $20.38 and $34.04 per hour, depending on experience, location, and employer.

What is a medical device integration?

A Medical Device Integration job involves connecting medical devices to healthcare IT systems, such as electronic health records (EHRs), to ensure seamless data exchange. Professionals in this role configure, test, and troubleshoot interfaces between devices and software to improve clinical workflows and patient care. They work closely with biomedical engineers, IT specialists, and healthcare providers to ensure reliable and accurate data transmission. Strong technical knowledge of interoperability standards like HL7, DICOM, and FHIR is often required.

What are some common challenges faced in medical device integration roles?

Professionals in Medical Device Integration often encounter challenges such as managing compatibility across diverse devices and systems, troubleshooting intermittent connectivity issues, and complying with strict health data security regulations. The role frequently involves working with cross-functional teams, including IT, clinical staff, and device manufacturers, which requires clear communication and collaboration. Additionally, the rapid pace of technological advancements means team members must continually update their knowledge and adapt to new standards. Overcoming these challenges is not only rewarding but also critical to delivering seamless interoperability and improving clinical workflows.

What are the key skills and qualifications needed to thrive in medical device integration?

To thrive in Medical Device Integration, you need a solid understanding of medical devices, networking, HL7 interfaces, and healthcare IT systems, often supported by a degree in biomedical engineering, information technology, or a related field. Familiarity with integration engines (such as Mirth Connect or Cloverleaf), EHR platforms, and relevant certifications like CBET or CHTM is highly beneficial. Strong problem-solving, teamwork, and communication skills help in collaborating with clinicians, vendors, and IT staff. These competencies are essential for ensuring reliable and secure data flow between devices and healthcare systems, ultimately supporting patient care and operational efficiency.

What cities in Texas are hiring for Medical Device Integration jobs?

Cities in Texas with the most Medical Device Integration job openings:

Infographic showing various Medical Device Integration job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $57,834 per year, or $27.8 per hour.

Systems Integration & Controls Engineer

Signature Science LLC

Austin, TX • On-site

$95K/yr

Full-time

Re-posted 5 days ago


Job description

Normal 0 false false false EN-US X-NONE X-NONE
Position Purpose:
Are you ready to make a meaningful difference in public health and national security? Signature Science is seeking a highly motivated and skilled Systems Integration & Controls Engineer to join our dedicated team. This pivotal role offers you the opportunity to contribute directly to complex R&D initiatives safeguarding national defense and enhancing biological safety. Your primary focus will be serving as the master integrator for a novel, clinical-grade In Vitro Diagnostic (IVD) sample preparation and testing device. This device bridges the gap between physical hardware, biology, and data systems. In this role, you will act as a lead in system integration, orchestrating technical deliverables between internal mechanical engineers and external electrical engineering subcontractors, and ensuring the entire instrument functions seamlessly as a unified platform. Additionally, you will serve as a core engineering resource across the company, applying your skills to a diverse portfolio of broader systems engineering and hardware integration projects.
Essential Duties and Responsibilities:
  • Act as a system integrator, ensuring flawless interoperability between prototype mechanical hardware, electrical architectures, fluidics, and control software.
  • Design and implement control architectures and automation strategies for prototype microfluidic and automated fluid-handling instruments, working closely with mechanical engineers and molecular biologists.
  • Define, manage, and debug technical interfaces, communication protocols, and APIs between external electrical engineering subcontractor deliverables and internal system components.
  • Integrate sensors, actuators, and other specialized equipment into both bespoke and pre-existing industrial or laboratory control architectures.
  • Work with multidisciplinary teams including a Principal Investigator, Quality/PM lead, and bioinformaticians to develop rigorous testing procedures, system verification protocols, and quality control methods to ensure consistent device performance.
  • Troubleshoot, debug, and solve complex electro-mechanical, fluidic, and system-level issues, utilizing industry best practices to analyze performance data.
  • Support broader company-wide systems engineering efforts, providing electrical, controls, and hardware integration expertise across various cross-functional project teams.
  • Contribute to the development and maintenance of laboratory standard operating procedures (SOPs) and systems engineering documentation.
  • Identify novel research directions, contribute to technical proposal efforts, and explore potential funding opportunities.
  • Maintain accurate, detailed laboratory records and project documentation.
  • Present research findings and engineering updates at internal technical reviews and external client meetings.

Required Knowledge, Skills & Abilities:
  • Minimum 3-5 years of experience designing, integrating, testing, and troubleshooting control or system software strategies for prototype hardware, preferably related to microfluidics, lab-on-a-chip, or precision automated laboratory systems.
  • Demonstrated experience acting as a system integrator or technical bridge across multidisciplinary teams (e.g., mechanical, electrical, software, and biological sciences).
  • Proven ability to interface with, evaluate, and integrate hardware or electrical engineering deliverables provided by external subcontractors.
  • Demonstrated experience using microcontrollers, single-board computers (e.g., Arduino, Raspberry Pi, or similar), or PLCs to control, script, and automate physical systems.
  • Experience establishing and debugging serial and network communication protocols (e.g., I2C, SPI, UART, CAN, TCP/IP) for interfacing and data transfer.
  • Familiarity with systems engineering principles, including the translation of P&ID documentation, functional requirements, and flow diagrams into robust control algorithms.
  • Familiarity with sensors and actuators relevant to fluid handling and automation, including pressure sensors, flow sensors, valves, pumps, and temperature controllers.
  • Ability to collaborate effectively within cross-functional teams, including mechanical engineers, chemists, molecular biologists, and software developers.
  • Excellent troubleshooting, analytical, and detailed documentation skills for iterative prototyping, validation, and transfer to production.
  • Experience using emerging AI tools or agentic AI systems to achieve specific objectives in an engineering or laboratory environment.
  • Experience or willingness to participate in grant writing and technical report preparation.

Other Potential Relevant Experience:
  • Familiarity with software development lifecycles within regulated environments, specifically medical device or IVD software design controls (IEC 62304 / ISO 14971).
  • Experience establishing verification and validation (V&V) protocols intended for FDA or regulatory submissions.
  • Proficiency with circuit design, schematic capture, PCB layout, and hands-on soldering and assembly skills to support the transition of R&D prototypes into robust systems.

Education/Experience:
  • Bachelor's degree or higher in Systems Engineering, Mechatronics, Electrical Engineering, Controls Engineering, Biomedical Engineering, or a related discipline.

Certificates/Licenses:
  • None required

Clearance:
  • This position requires that the candidate be willing and able to complete a successful background screening for a security clearance. Candidates with an active security clearance will receive preference.

Supervisory Responsibilities:
  • None

Working Conditions/ Equipment:
This is a full-time, fully on-site position. This position primarily operates during standard business hours, with occasional needs for extended workdays or weekend work to meet project timelines. A significant portion of this role (approximately 50%) involves hands-on laboratory work and benchtop engineering. You should be comfortable spending extended periods of time conducting hardware experiments and working at a computer. The role may also require occasional domestic travel for conferences, client meetings, or research-related travel. The ability to lift and carry light loads (under 25 lbs) without assistance is necessary.