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Remote International Biomedical Engineer Jobs in Riverside, CA

Moderna

Intern, CMC Development (Summer 2027)

Pomona, CA · On-site +1

$20 - $60/hr

... remote work . Here's What You'll Do * Work with a team of highly skilled experts to come up to ... Engineering, Chemistry, Biochemistry, Biomedical Engineering, Biophysics, Biostatistics ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

Perform remote monitoring activities such as source data verification (SDV) and data entry checks ... biomedical engineering). * 5+ years of clinical research experience at a Sponsor, preferably in ...

ABB

Senior Project Engineer

La Verne, CA · Remote

$101K - $132K/yr

The work model for this role is: Remote {#LI-Remote} This role is contributing to the ... Comfortable with up to 50% travel (domestic and international). Preferred Skills * Experience with ...

ABB

Senior Project Engineer

Irvine, CA · Remote

$101K - $132K/yr

The work model for this role is: Remote {#LI-Remote} This role is contributing to the ... Comfortable with up to 50% travel (domestic and international). Preferred Skills * Experience with ...

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All JobsInternational Biomedical Engineer JobsRemote International Biomedical Engineer JobsRemote International Biomedical Engineer Jobs in Riverside, CA

Remote International Biomedical Engineer information

See Riverside, CA salary details

$42.8K

$98.9K

$146.1K

How much do remote international biomedical engineer jobs pay per year?

As of Sep 13, 2026, the average yearly pay for remote international biomedical engineer in Riverside, CA is $98,909.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,700.00 and $121,000.00 per year, depending on experience, location, and employer.

What is a remote international biomedical engineer?

A Remote International Biomedical Engineer is a professional who works from a location outside of a traditional office or laboratory, often from another country, to support the design, development, maintenance, and troubleshooting of medical equipment and devices. Their responsibilities typically include collaborating with global teams, providing technical support to healthcare facilities, ensuring regulatory compliance, and assisting with product installations and training remotely. This role requires strong communication skills, technical expertise in biomedical engineering, and familiarity with international standards and regulations. Remote work allows them to assist clients and colleagues across different countries without needing to be physically present.

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

To thrive as a Remote International Biomedical Engineer, you need a strong background in biomedical engineering principles, troubleshooting medical devices, and typically a relevant engineering degree. Familiarity with industry-standard tools such as CAD software, medical device regulations (FDA, CE), and remote collaboration platforms is essential. Excellent problem-solving, cross-cultural communication, and self-motivation are standout soft skills for this role. These skills ensure effective design, compliance, and support of medical technologies across diverse global environments while working remotely.

How does a remote international biomedical engineer collaborate effectively with global teams and clients across different time zones?

As a Remote International Biomedical Engineer, collaboration with colleagues and clients worldwide is typically managed through virtual meetings, project management platforms, and clear communication protocols. Flexibility in scheduling is often necessary to accommodate time zone differences, and regular updates are essential to keep all stakeholders aligned. Building strong relationships through proactive communication and cultural sensitivity helps ensure smooth teamwork and project success. Many organizations also provide tools and resources to support seamless international collaboration, such as shared documentation systems and multilingual support.

What is the difference between Remote International Biomedical Engineer vs Remote International Medical Device Technician?

AspectRemote International Biomedical EngineerRemote International Medical Device Technician
Required CredentialsBiomedical engineering degree, certifications in medical device regulationTechnical certifications, device-specific training
Work EnvironmentDesign, development, and testing of medical devices remotelyInstallation, maintenance, and troubleshooting remotely
Employer & Industry UsageHospitals, medical device companies, research institutionsMedical device manufacturers, healthcare providers

Remote International Biomedical Engineers focus on designing and developing medical devices, often requiring engineering degrees and regulatory knowledge. In contrast, Remote International Medical Device Technicians primarily handle installation, maintenance, and troubleshooting of devices. Both roles are essential in healthcare technology, but they differ in responsibilities and skill sets.

What are popular job titles related to Remote International Biomedical Engineer jobs in Riverside, CA?

For Remote International Biomedical Engineer jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Remote International Biomedical Engineer jobs in Riverside, CA look for?

The top searched job categories for Remote International Biomedical Engineer jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Remote International Biomedical Engineer jobs?

Cities near Riverside, CA with the most Remote International Biomedical Engineer job openings:

Remote International Biomedical Engineer jobs near you
Infographic showing various Remote International Biomedical Engineer job openings in Riverside, CA as of August 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 100% Remote job distribution, with an average salary of $98,909 per year, or $47.6 per hour.

Quality Assurance Engineer (ISO 13485)

Irvine, CA • On-site, Remote

Prismatik
See more jobs at Prismatikexternal

$70K - $100K/yr

Full-time

Posted 4 days ago

Job description

We're looking for aQuality Assurance Engineerto help build quality into every stage of our medical device development and manufacturing. You'll have broad ownership across quality engineering, risk management, CAPA, validation, and our Quality Management System. Working closely with cross-functional teams, you'll solve complex quality challenges, support new products and processes, and help ensure what we build meets the highest standards for safety, performance, and compliance.
Essential Functions:
  • Conducts engineering activities in compliance with FDA Regulations, ISO 13485, and other national and international quality and regulatory requirements and standards.
  • Leads product quality assurance and quality engineering activities to drive strong engineering and technical knowledge.
  • Creates quality assurance, engineering programs, and initiatives to ensure products are developed and manufactured according to applicable requirements.
  • Collaborates on investigations of NCR's and complaints as necessary; suggests corrective and preventive actions based on engineering analysis and review; suggests effective solutions to drive continuous and measurable improvements.
  • Works with various departments to ensure highest quality products and processes are developed, deployed, and meet all engineering requirements; activities include but not limited to product design testing, process testing, characterization, qualification, validation, and risk analysis/FMEA.
  • Collaborates to create systems for the identification, analysis, correction, and prevention of quality issues; identifies areas for improvement as needed.
  • Participates in quality engineering projects from inception to deployment.
  • Participates in CAPA Management and other quality engineering projects.
  • Participates in trainings for quality engineering tools within the organization using ISO 14971.
  • Collaborates with team members to provide technicians and R&D personnel to provide technical leadership in problem resolution, process streamlining, and continuous improvement activities.
  • Analyzes data and trends; reports results to management.
  • Collaborates with team members to complete failure investigations and root cause analysis.
  • Collaborates in design verification testing for design control projects.
  • Performs returned product analysis and failure investigation activities.
  • Ensures procedures and regulations are adequately followed during NCMR process.
  • Ensures calibration and preventive management systems meet compliance requirements.
  • Identifies the optimization of complex manufacturing processes using engineering methods for manufacturing design and continuous process improvement.
  • Identifies opportunities for re-design and/or design of more complex equipment, tools, and fixtures to improve manufacturing processes and reduce risk.
  • Performs other related duties and projects as business needs require at direction of management

Minimum Qualifications:

  • Bachelor's degree in Science, Engineering, or related field; or equivalent combination of experience and training; advanced degree preferred
  • Minimum three (3) years of experience in quality engineering and risk management.
  • Knowledge of FDA regulations, ISO 13485, and other applicable international quality standards.
  • Knowledge of risk management (ISO 14971), design controls, and validation methodologies.
  • Proven analytical, problem-solving, and communication skills.
  • Proficiency in quality and statistical analysis tools such as Minitab or equivalent software.
  • Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or Six Sigma certification, preferred.
  • Experience with combination products or Class I/II medical devices, preferred.
  • Familiarity with EU MDR and UDI regulatory requirements, preferred.
Pay range: $70,000.00 - $100,000/yr.
Exact compensation may vary based on skills and experience.
This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.
Employment Type: full-time

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