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International Biomedical Engineer Jobs in Texas (NOW HIRING)

Craig Technologies

Human Performance Engineer

Houston, TX · On-site

$65K - $80K/yr

... Biomedical Research and Environmental Sciences Division at NASA Johnson Space Center. Our work ... International Space Station, Gateway, Human Landing System and Orion. Your work will be cross ...

Spectral MD Inc

Cybersecurity Engineer

Dallas, TX · On-site

... international standards (e.g.. ANSI/AAMI SW 96:2003, IEC 62304, IEC 81001, ISO 14971, ISO 27001 ... Biomedical Engineering, Data Science, Systems Engineering, and IT internal teams to embed ...

Enovis

Sr. Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Manufacturing Engineering, or ... international regulations. * Demonstrated experience supporting new product development using ...

Cedarparktexasedc

Sr. Quality Engineer

Austin, TX · On-site

$120 - $180/hr

Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Manufacturing Engineering, or ... international regulations. * Demonstrated experience supporting new product development using ...

Enovis

Sr. Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Manufacturing Engineering, or ... international regulations. * Demonstrated experience supporting new product development using ...

Artidis

Field Service Software Engineer

Houston, TX · On-site

Qualifications * Bachelor's degree in Computer Science, Software Engineering, Biomedical ... international team. Our company is an excellent place for rapid advancement and offers a promising ...

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All JobsInternational Biomedical Engineer JobsInternational Biomedical Engineer Jobs in Texas

International Biomedical Engineer information

See Texas salary details

$38.2K

$88.3K

$130.4K

How much do international biomedical engineer jobs pay per year?

As of Aug 24, 2026, the average yearly pay for international biomedical engineer in Texas is $88,327.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,400.00 and $108,100.00 per year, depending on experience, location, and employer.

What does an international biomedical engineer do?

An International Biomedical Engineer designs, develops, and maintains medical equipment and devices used in healthcare settings around the world. They often work with cross-border teams to ensure medical technologies meet international standards and can be effectively used in diverse environments. Their responsibilities also include training healthcare staff, troubleshooting equipment issues, and ensuring compliance with global regulations. International Biomedical Engineers play a crucial role in improving healthcare delivery and patient outcomes worldwide.

What are the key skills and qualifications needed to thrive as an international biomedical engineer?

To thrive as an International Biomedical Engineer, you need a strong background in biomedical engineering principles, an accredited engineering degree, and knowledge of international regulatory standards. Familiarity with medical device design software, quality management systems like ISO 13485, and relevant certifications such as Certified Biomedical Equipment Technician (CBET) are often required. Excellent cross-cultural communication, adaptability, and problem-solving skills help professionals excel in diverse global environments. These competencies are crucial for ensuring the safe, compliant, and effective use of medical technologies across international healthcare markets.

What are some common challenges faced by international biomedical engineers when working with healthcare facilities in different countries?

International Biomedical Engineers often encounter challenges such as adapting to varying healthcare regulations, standards, and languages across countries. Navigating logistical issues like equipment import/export, local infrastructure limitations, and diverse cultural expectations can also be demanding. Successful engineers typically develop strong cross-cultural communication skills and stay up-to-date on international compliance requirements to effectively support global projects and ensure patient safety.

What is the difference between International Biomedical Engineer vs Clinical Biomedical Engineer?

AspectInternational Biomedical EngineerClinical Biomedical Engineer
CredentialsBachelor's or Master's in Biomedical Engineering, certifications vary by countryBachelor's or Master's in Biomedical Engineering, often with clinical certifications
Work EnvironmentGlobal settings, including manufacturing, research, and international projectsHospitals, clinics, and healthcare facilities
Employer & IndustryMedical device companies, research institutions, international organizationsHospitals, healthcare providers, medical device service companies

International Biomedical Engineers typically work in global or cross-border settings, focusing on product development and international projects, while Clinical Biomedical Engineers work directly within healthcare facilities, maintaining medical equipment and ensuring patient safety. Both roles require biomedical engineering knowledge but differ mainly in work environment and focus.

What are the most commonly searched types of International Biomedical Engineer jobs in Texas?

The most popular types of International Biomedical Engineer jobs in Texas are:

What are popular job titles related to International Biomedical Engineer jobs in Texas?

For International Biomedical Engineer jobs in Texas, the most frequently searched job titles are:

What job categories do people searching International Biomedical Engineer jobs in Texas look for?

The top searched job categories for International Biomedical Engineer jobs in Texas are:

International Biomedical Engineer jobs near you
Infographic showing various International Biomedical Engineer job openings in Texas as of August 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $88,327 per year, or $42.5 per hour.

Clinical Research Associate (Biomedical Engineering Candidates)

Medpace, Inc.

Irving, TX • On-site

Other

Medical, Retirement, PTO

Posted 24 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research

Job description

Job Summary
Join our CRA Team in Dallas, TX!
We are hiring those with Biomedical Engineering backgrounds for the CRA role!
The Clinical Research Associate position offers an exciting career within clinical research! For those with biomedical engineering backgrounds wanting to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this is the right opportunity for you!
This position is office based in Dallas, TX.
Medpace CRA Training Program (PACE®)
No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. The PACE® (Professionals Achieving CRA Excellence) Training Program includes the following:
  • A platform to effectively and confidently carry out CRA duties to ultimately become a high-functioning, independent, Medpace CRA
  • Interactive discussions with hands-on exercises and practicums
  • Core departmental rotations to learn various aspects of the drug/device development and approval process

Why CRA?
  • Exciting travel opportunities
  • Make a difference on a larger scale through the development of medical drugs and devices
  • Dynamic working environment with varying day-to-day responsibilities
  • Exposure to multiple therapeutic areas
  • Defined CRA promotion and growth ladder

We Offer the Following:
  • Competitive travel bonus
  • Equity/Stock option program
  • Training completion and retention bonus
  • Annual merit increases
  • 401K matching
  • Opportunity to work from home
  • Flexible work hours across days within a week
  • Retain airline reward miles and hotel reward points
  • Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
  • In-house travel agents, reimbursement for airline club membership, and TSA pre-check
  • Opportunity for leadership positions - Lead CRA, CRA Manager, Training and Development Manager, and many more
  • CRA training program - PACE®
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
  • In-house administrative support for all levels of CRA
  • Opportunity to work with international team of CRAs

Responsibilities
  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
  • On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward
  • Verification the investigator is enrolling only eligible subjects
  • Regulatory document review
  • Medical device and/or investigational product/drug accountability and inventory
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
  • Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications
  • Minimum of a Bachelor's degree in a health or science related field; degree in Biomedical Engineering preffered
  • Ability to travel 60-70% to locations nationwide is required
  • A valid driver's license and the ability to drive to monitoring sites
  • Minimum 1 year healthcare-related work experience preferred
  • Proficient knowledge of Microsoft Office
  • Strong communication and presentation skills
  • Detail-oriented and efficient in time management

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events

Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

What Medpace employees say

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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