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Remote International Medical Scribe Jobs in Riverside, CA

Wayvia

Customer Support Specialist

Irvine, CA · Remote

$21 - $23/hr

Wayvia is an international employer so some benefits offering will vary from country to country ... Medical/Dental/Vision * 16 weeks of paid parental leave (US) * Technical stipend * Professional ...

Aprio

Tax Manager

Irvine, CA · On-site +1

$108K - $148K/yr

S. office locations, as well as international office locations and more than 3,200 team members ... Perks/Benefits we offer for full-time team members: - Medical, Dental, and Vision Insurance on the ...

Clydeco

Associate Attorney, Aviation Group

Irvine, CA · On-site +1

$2.0K/mo

The role can also be fully remote from anywhere in California. Responsibilities Specific ... Comprehensive Health Benefits - Medical, dental, and vision coverage for you and your family.

Bourns, Inc.

Manager Customer Service

Riverside, CA · On-site +1

... medical, and other markets. Our commitment to innovation, quality, and customer service has made us ... including remote and international team members. * Establish departmental goals, monitor ...

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All JobsInternational Medical Scribe JobsRemote International Medical Scribe JobsRemote International Medical Scribe Jobs in Riverside, CA

Remote International Medical Scribe information

See Riverside, CA salary details

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$19

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How much do remote international medical scribe jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for remote international medical scribe in Riverside, CA is $19.05, according to ZipRecruiter salary data. Most workers in this role earn between $15.82 and $21.30 per hour, depending on experience, location, and employer.

What is a remote international medical scribe?

A Remote International Medical Scribe is a professional who assists healthcare providers by documenting patient encounters in real-time from a remote location, often in a different country than where the healthcare provider is based. Their main responsibility is to enter accurate and detailed medical information into electronic health records (EHRs) during patient visits, allowing physicians to focus more on patient care. Remote international scribes work virtually, using secure technology to access charts and communicate with providers, and must have a strong understanding of medical terminology and clinical workflows. This role helps improve the efficiency and accuracy of medical documentation in healthcare settings.

How do remote international medical scribes typically collaborate with healthcare providers across different time zones?

Remote International Medical Scribes often work with physicians and clinical teams located in different countries, which means managing time zone differences is a common aspect of the job. Most employers provide flexible scheduling, but effective communication and punctuality are crucial to ensure live documentation during patient visits. Scribes use secure telemedicine platforms and electronic health record (EHR) systems to coordinate in real time, and may join virtual meetings or communicate asynchronously depending on the provider's workflow. Being proactive in clarifying schedules and adapting to changing time slots can help build trust and efficiency within the team.

What are the key skills and qualifications needed to thrive as a remote international medical scribe, and why are they important?

To thrive as a Remote International Medical Scribe, you need a strong grasp of medical terminology, accurate documentation skills, and typically a background in life sciences or healthcare. Familiarity with electronic health records (EHR) systems, medical transcription software, and HIPAA compliance is essential. Excellent written communication, attention to detail, and the ability to multitask in a virtual environment are standout soft skills. These competencies ensure precise clinical documentation, streamline physician workflows, and uphold patient privacy standards in remote healthcare settings.

What are the most commonly searched types of International Medical Scribe jobs in Riverside, CA?

The most popular types of International Medical Scribe jobs in Riverside, CA are:

What are popular job titles related to Remote International Medical Scribe jobs in Riverside, CA?

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

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

The top searched job categories for Remote International Medical Scribe jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Remote International Medical Scribe jobs?

Cities near Riverside, CA with the most Remote International Medical Scribe job openings:

Remote International Medical Scribe jobs near you
Infographic showing various Remote International Medical Scribe job openings in Riverside, CA as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $39,632 per year, or $19.1 per hour.

Sr. Quality Assurance Engineer (ISO 13485)

Prismatik

Irvine, CA • On-site, Remote

$99K - $120K/yr

Full-time

Posted 4 days ago

Job description

We're looking for a Sr. QA Engineer to 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:
  • Ensure compliance with applicable regulatory standards, including FDA 21 CFR Part 820, ISO 13485, MDSAP, and EU MDR.
  • Lead and support CAPA investigations, non-conformance management, and root cause analysis using tools such as 8D, Fishbone, and 5 Whys.
  • Own and continuously improve elements of the Quality Management System (QMS), including document control, internal audits, supplier quality, and change control.
  • Collaborate cross-functionally with R&D, Manufacturing, and Regulatory Affairs to support design control, risk management (ISO 14971), and product development lifecycle activities.
  • Lead internal and supplier audits, and support external audits and inspections (e.g., FDA, Notified Bodies).
  • Participate in validation activities (IQ/OQ/PQ) for processes, equipment, and software used in manufacturing and quality operations.
  • Develop, monitor, and analyze quality metrics to identify trends, drive continuous improvement, and ensure effectiveness of corrective actions.
  • Provide quality engineering support to Quality Control, including guidance on inspection methods, metrology, and measurement system capability.
  • Conduct and document investigations of NCRs, complaints, and deviations, providing effective and sustainable corrective and preventive actions based on engineering analysis.
  • Lead and mentor junior engineers, fostering technical growth and reinforcing a culture of quality and compliance.
  • Integrate ISO 14971 risk management and IEC 62366 usability engineering activities within Glidewell/Prismatik processes.
  • Ensure organizational compliance with the QMS through ongoing training, education, and internal communication.
  • Collaborate with Manufacturing and Engineering to coordinate pilot production, process validations, and risk analyses for new products and processes.
  • Ensure calibration and preventive maintenance systems meet compliance and operational requirements.
  • Identify and implement process optimizations using Lean and Six Sigma methodologies to improve manufacturability, reduce risk, and enhance efficiency.
  • Identify opportunities for design or re-design of equipment, tools, and fixtures to improve manufacturing processes and product quality.
  • Perform other related duties and special projects as assigned by management.
Minimum Qualifications:
  • Bachelor's degree in Engineering, Science, or a related technical field.
  • Minimum of 5 years of experience in Quality Assurance or Quality Engineering within the medical device industry, or equivalent education and experience demonstrating comparable skills and knowledge.
  • Strong working knowledge of FDA regulations, ISO 13485, and other applicable international quality standards.
  • Hands-on experience with 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.
  • Demonstrated project management experience.
  • 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: $99,000 - $120,000/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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