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International Remote Biomedical Jobs in Riverside, CA

Sr. Program Manager

Irvine, CA · On-site +1

$124K - $125K/yr

Willingness to travel 10-20% (domestic and international) * Proficiency in Excel, financial ... Remote or field-based positions will have different workplace arrangements which will be indicated ...

International Remote Biomedical information

See Riverside, CA salary details

$16

$29

$40

How much do international remote biomedical jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for international remote biomedical in Riverside, CA is $29.76, according to ZipRecruiter salary data. Most workers in this role earn between $25.34 and $33.61 per hour, depending on experience, location, and employer.

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

AspectInternational Remote BiomedicalInternational Remote Medical Laboratory Technician
Required CredentialsBachelor's in Biomedical Science or related field, certifications varyAssociate's or Bachelor's in Medical Laboratory Technology, relevant certifications
Work EnvironmentRemote, research-focused, data analysisRemote, laboratory data processing, sample management
Employer & Industry UsageResearch institutions, biotech companies, healthcareHospitals, diagnostic labs, healthcare providers
Common Search & ComparisonYesNo

International Remote Biomedical roles typically involve research, data analysis, and development in biotech or healthcare sectors, requiring a biomedical background. In contrast, International Remote Medical Laboratory Technicians focus on lab data management and sample processing, often needing specific laboratory technology certifications. Both roles are remote and industry-related but differ in daily tasks and credential requirements.

What is an International Remote Biomedical professional?

An International Remote Biomedical professional is someone who works in the biomedical field, such as biomedical engineering or research, while operating remotely from a location different from where the healthcare or research facility is based. These professionals may collaborate with global teams to develop, test, or maintain medical devices, analyze biomedical data, or support healthcare technology projects across borders. Their work often involves using digital tools and communication platforms to bridge geographical gaps, ensuring effective contribution to international biomedical projects.

What are the key skills and qualifications needed to thrive as an International Remote Biomedical Specialist, and why are they important?

To thrive as an International Remote Biomedical Specialist, you typically need a degree in biomedical engineering or a related field, along with strong analytical and problem-solving skills. Familiarity with medical device software, remote diagnostic tools, and international regulatory standards is highly valuable. Excellent communication, cultural sensitivity, and self-motivation are crucial soft skills for collaborating across global teams and supporting clients remotely. These competencies ensure effective technical support, regulatory compliance, and seamless operations in diverse, international healthcare environments.

What are some common challenges faced by International Remote Biomedical professionals, and how can they be addressed?

International Remote Biomedical professionals often face challenges such as coordinating across different time zones, navigating diverse regulatory requirements, and ensuring effective communication with global teams. To address these, it's important to utilize robust digital collaboration tools, stay updated on international compliance standards, and develop strong cross-cultural communication skills. Regular virtual meetings, clear documentation, and a proactive approach to problem-solving can further help maintain project momentum and foster successful international collaborations.
What are popular job titles related to International Remote Biomedical jobs in Riverside, CA? For International Remote Biomedical jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching International Remote Biomedical jobs in Riverside, CA look for? The top searched job categories for International Remote Biomedical jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for International Remote Biomedical jobs? Cities near Riverside, CA with the most International Remote Biomedical job openings:
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 • On-site, Remote

$160K - $210K/yr

Other

Medical, Dental, Vision, Retirement, PTO

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