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Remote International Biomedical Engineer Jobs in Riverside, CA

Remote in the United States. Candidates MAY NOT be located in the following states: AL, CO, DE, HI ... Proven project experience specifically in healthcare and/or biomedical engineering. * Exceptional ...

Clinical Research Associate

Irvine, CA ยท 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 ...

Senior Project Engineer

Irvine, CA ยท Remote

$105K - $136K/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 ...

Senior Project Engineer

La Verne, CA ยท Remote

$98K - $128K/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 ...

Senior ITS Engineer

Irvine, CA ยท On-site +1

$163K - $278K/yr

You'll collaborate with local offices and international teams, contributing to high-impact ... S. This is a remote position: candidates can sit out of any U.S. WSP office. California PE ...

Data Engineer III

Irvine, CA ยท On-site +1

$160K - $180K/yr

Wayvia is an international employer so some benefits offering will vary from country to country ... This is a remote position open to candidates based in the United States. Compensation: The salary ...

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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 Jul 14, 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 are the key skills and qualifications needed to thrive as a Remote International Biomedical Engineer, and why are they important?

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 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 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 the most commonly searched types of International Biomedical Engineer jobs in Riverside, CA? The most popular types of International Biomedical Engineer jobs in Riverside, CA are:
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:
Infographic showing various Remote International Biomedical Engineer job openings in Riverside, CA as of July 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% Remote job distribution, with an average salary of $98,909 per year, or $47.6 per hour.
Head of Operations and Manufacturing - Medical Device (Hybrid or Remote)

Head of Operations and Manufacturing - Medical Device (Hybrid or Remote)

Canon Recruiting Group

Irvine, CA โ€ข On-site, Remote

$160K - $210K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 21 days ago


Job description

Head of Operations and Manufacturing | California (Hybrid or Remote) | Full-Time

POSITION SUMMARY

The Head of Operations and Manufacturing will own the end-to-end operational infrastructure required to bring our FDA-regulated cuffless blood pressure monitor to market and scale production. This is a hands-on leadership role for someone who thrives building from zero to one in a regulated environment: selecting contract manufacturers, standing up supply chains compliant with FDA 21 CFR Part 820, establishing ISO 13485-certified quality management systems, and preparing for direct-to-patient fulfillment.

As a company preparing for 510(k) submission and commercial launch, this role is critical to ensuring we can reliably manufacture and deliver a high-quality, FDA-cleared medical device at scale. The ideal candidate brings deep experience in medical device manufacturing (particularly wearable or electro-optical devices), understands regulated hardware supply chains and design transfer, and can roll up their sleeves while building the team and processes for long-term growth.

This position reports directly to the CEO with high visibility to the leadership team and Board of Directors.

KEY RESPONSIBILITIES

Manufacturing & Production

  • Lead selection and onboarding of contract manufacturing partners with Class II medical device experience, including RFQ, quality audits, contract negotiation, and ongoing management.
  • Own design transfer and manufacturing transfer, working with engineering on DFM principles, Device Master Record (DMR) requirements, and production readiness.
  • Establish production planning, forecasting, and capacity management for V&V builds, pilot production, and volume manufacturing.
  • Drive continuous improvement in yield, quality, and cost while maintaining FDA and ISO compliance.
  • Oversee pilot runs and scale-up, including process validation (IQ/OQ/PQ) and manufacturing controls.

Supply Chain & Procurement

  • Build and manage the end-to-end supply chain, including component sourcing, supplier qualification, and inventory management per FDA purchasing controls.
  • Develop supplier relationships and negotiate terms while ensuring supply continuity, traceability, and risk mitigation.
  • Implement inventory planning to balance working capital with service levels, including buffer strategies for Year 1 launch.
  • Monitor and mitigate supply chain risks: component shortages, single-source dependencies, geopolitical factors, and logistics disruptions.

Quality & Regulatory Compliance

  • Maintain and improve the ISO 13485-certified QMS in partnership with the quality and regulatory team, ensuring FDA 21 CFR Part 820 compliance.
  • Support 510(k) submission activities related to manufacturing, including process validation documentation, DMR development, and device history records (DHR).
  • Define incoming inspection, in-process controls, and final product testing consistent with the risk management file.
  • Manage product certifications for a Class II device, including FDA registration, UDI compliance, and applicable international requirements.
  • Lead root cause analysis and CAPA for quality issues, ensuring post-market surveillance compliance.

Fulfillment & Logistics

  • Design the direct-to-patient fulfillment strategy, including 3PL selection with FDA-cleared Class II device experience.
  • Establish logistics and distribution for nationwide shipping of a regulated device with chain-of-custody and traceability.
  • Develop returns, replacement, and warranty processes that balance patient experience, cost, and compliance.

Team & Organizational Development

  • Start as an individual contributor who executes hands-on, then build and lead the operations team through 510(k) clearance and commercial launch.
  • Establish operational metrics and dashboards for manufacturing, supply chain, and quality performance.
  • Partner with finance on cost modeling, COGS optimization, and operational budgeting.
  • Collaborate cross-functionally with engineering, software, regulatory, and commercial teams.


QUALIFICATIONS

  • 7-12 years in manufacturing, operations, or supply chain, with 3-5+ years in medical devices (Class II preferred), wearables, or regulated hardware.
  • Experience managing contract manufacturers for regulated medical devices, preferably in Asia and/or domestically.
  • Experience at or with CMs/EMS providers (Flex, Jabil, Celestica, Plexus, Sanmina) in Class II medical device or wearable programs is a strong plus.
  • Track record of design transfer and scaling production from pilot to volume for regulated products.
  • ISO 13485 and FDA 21 CFR Part 820 experience required.
  • Familiarity with the 510(k) process and manufacturing documentation (process validations, DMR/DHR) strongly preferred.
  • Bachelor's in Engineering, Supply Chain, Operations, Biomedical Engineering, or related field; MBA or advanced degree a plus.
  • Based in California or travel up to 25%.

COMPENSATION

  • Base Salary: $160,000 - $210,000 USD
  • Performance Bonus: Tied to company milestones and personal objectives
  • Equity: Early-stage stock option grant with meaningful ownership
  • 100% Employer-Paid Healthcare: Medical, dental, and vision
  • Additional Benefits: 401(k) with company match, flexible PTO

WORKING CONDITIONS:

  • May on occasion be exposed to loud sounds and distracting noise levels, such as from office equipment.
  • The ability to lift up to 30lbs
  • Use of computers and technology

Here at Canon Recruiting, People are our priority, and we are committed to Include Diversity in every segment of who we are. It is only through our Diversity; we are made a stronger organization and increase our ability to provide top tier candidates that our clients have come to know Canon for. We have an inclusive environment all employees are celebrated for their unique differences. The different perspectives and experiences of our workforce give us the competitive advantage that is essential for success in an ever-changing market. By promoting inclusion with the same enthusiasm, we devote to quality and competency and using the experience from a diverse assortment of backgrounds and experiences, Canon can improve the services and value we deliver to clients, employees, and customers. At Canon, Diversification and Inclusiveness are much more than a corporate ambition; they are a critical component in our daily corporate life. Canon Recruiting is committed to a diverse and inclusive workplace. Canon Recruiting is an equal opportunity employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. The pay range for this position is listed above. Base pay information is based on market location. We will consider for employment qualified applicants with arrest and conviction records. Our range of benefits may include health care and 401(k) savings plans. For individuals with disabilities who would like to request an accommodation, please email hr@canonrecruiting.com