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Remote Quality Engineer Medical Device Jobs in Santa Rosa, CA

GCX Healthcare Solutions

Software Engineer

Petaluma, CA · Remote

$125K - $150K/hr

As part of GCX, a leader in medical carts and medical mounting solutions, Lilitab combines ... Develop webview-based device UIs with JavaScript-to-native/system integrations * Design and ...

Doxel

Staff Software Engineer, Full Stack

Bodega Bay, CA · Remote

$200K - $250K/yr

... IoT device outputs--and transform them into fast, intuitive workflows for both office teams and ... Remote first culture (for most roles) * Comprehensive Health Insurance (Medical, Dental, Vision)

W3Global Inc.

Civil Engineer

Santa Rosa, CA · On-site +1

$110K - $150K/yr

We are full service professional civil and environmental engineering firm with over 50 years of ... Remote Work Capability * 100% Employee Medical * Dental/Vision * 401k w\matching * Paid Vacation ...

Anchor Health

Remote Hospice Billing Supervisor

Petaluma, CA · Remote

$61K - $80K/yr

Collaborate with other departments, including admissions, compliance, and medical records, to ... Participate in continuous quality improvement initiatives to enhance billing processes and patient ...

New

ABB

Protection and Control Engineer

CA · Remote

While this is a full remote position, there is preference for candidates located in the Northern ... Choice between two medical plan options: A PPO plan called the Copay Plan OR a High Deductible ...

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All JobsQuality Engineer Medical Device JobsRemote Quality Engineer Medical Device JobsRemote Quality Engineer Medical Device Jobs in Santa Rosa, CA

Remote Quality Engineer Medical Device information

See Santa Rosa, CA salary details

$49.2K

$91.9K

$130.1K

How much do remote quality engineer medical device jobs pay per year?

As of Aug 8, 2026, the average yearly pay for remote quality engineer medical device in Santa Rosa, CA is $91,883.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,700.00 and $101,700.00 per year, depending on experience, location, and employer.

What does a remote quality engineer in the medical device industry do?

A Remote Quality Engineer in the medical device industry is responsible for ensuring that medical products meet regulatory and quality standards while working from a remote location. Their duties often include reviewing and improving quality processes, conducting audits, analyzing data to identify trends or issues, and ensuring compliance with regulations such as FDA or ISO 13485. They collaborate with cross-functional teams to resolve quality issues and may also be involved in risk management and validation activities. Remote Quality Engineers use digital tools to communicate and manage documentation, making it possible to fulfill their role away from a traditional office or manufacturing environment.

What are the key skills and qualifications needed to thrive as a remote quality engineer in medical devices, and why are they important?

To thrive as a Remote Quality Engineer in Medical Devices, you need a solid background in quality assurance, regulatory compliance (such as FDA and ISO 13485), and engineering principles, typically supported by a relevant engineering degree. Proficiency with quality management systems (QMS), document control software, and risk assessment tools is common, and certifications like ASQ CQE are highly valued. Strong attention to detail, effective problem-solving, and clear remote communication skills help ensure compliance and collaboration across distributed teams. These abilities are crucial for maintaining product safety, meeting regulatory standards, and driving continuous improvement in a regulated industry.

How does a remote quality engineer in the medical device industry effectively collaborate with cross-functional teams despite working off-site?

Remote Quality Engineers in the medical device sector regularly use digital collaboration tools such as video conferencing, shared documentation platforms, and cloud-based quality management systems to stay connected with design, manufacturing, and regulatory teams. While working remotely poses challenges in terms of immediate access to physical devices and face-to-face communication, frequent virtual meetings and clear documentation help ensure alignment on project goals and compliance requirements. Building strong relationships with on-site team members and proactively seeking feedback are key strategies for maintaining effective collaboration and ensuring product quality.
What are popular job titles related to Remote Quality Engineer Medical Device jobs in Santa Rosa, CA? For Remote Quality Engineer Medical Device jobs in Santa Rosa, CA, the most frequently searched job titles are:
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What cities near Santa Rosa, CA are hiring for Remote Quality Engineer Medical Device jobs? Cities near Santa Rosa, CA with the most Remote Quality Engineer Medical Device job openings:
Remote Quality Engineer Medical Device jobs near you
Infographic showing various Remote Quality Engineer Medical Device job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $91,883 per year, or $44.2 per hour.

Product Manager CPAP Masks and Interfaces (Remote)

SleepRes, Inc.

Bodega Bay, CA • Remote

$155K - $170K/yr

Full-time

Posted 8 days ago

Job description

Position Summary

We are seeking an experienced and customer-focused Product Manager to lead the strategy, development, and lifecycle management of our CPAP and respiratory mask portfolio. This role will be responsible for identifying market opportunities, translating user needs into innovative product solutions, and driving cross-functional execution from concept through commercialization.

The ideal candidate has experience in sleep therapy, respiratory care, medical devices, or patient interface products and possesses a strong understanding of user-centered design, regulatory requirements, and commercialization within healthcare markets.

Key Responsibilities

Product Strategy & Portfolio Management

  • Develop and execute product roadmaps for CPAP masks, respiratory interfaces, and related accessories.
  • Conduct market analysis to identify customer needs, competitive trends, and growth opportunities.
  • Define product requirements and business cases for new product development initiatives.
  • Manage the full product lifecycle, including product launches, enhancements, and end-of-life planning.
  • Monitor portfolio performance and recommend actions to improve market share, profitability, and customer satisfaction.

Voice of Customer & Market Insights

  • Gather and synthesize feedback from patients, sleep clinicians, respiratory therapists, DME providers, and healthcare systems.
  • Conduct customer interviews, usability studies, and field observations to identify unmet needs.
  • Translate clinical and user insights into actionable product requirements.
  • Partner with R&D , Marketing, Clinical Affairs, and Sales to understand market dynamics and reimbursement trends.

Product Development

  • Collaborate with Engineering, Industrial Design, Human Factors, Clinical, Regulatory, Quality, and Operations teams throughout development.
  • Define product specifications, user requirements, and acceptance criteria.
  • Support risk management, usability engineering, and validation activities.
  • Participate in design reviews and ensure products meet customer and regulatory expectations.

Commercialization & Launch

  • Develop product positioning, value propositions, and go-to-market strategies.
  • Support sales training and creation of customer-facing materials.
  • Partner with Marketing to develop launch plans and commercialization strategies.
  • Track launch performance and customer adoption metrics.

Cross-Functional Leadership

  • Serve as the primary product champion across the organization.
  • Lead cross-functional teams to achieve project milestones, timelines, and business objectives.
  • Facilitate alignment among stakeholders while balancing technical, commercial, and customer priorities.

Qualifications

Required

  • Bachelor's degree in Marketing, Business, Engineering, Life Sciences, or related field.
  • 3+ years of product management experience in medical devices, healthcare products, or respiratory care.
  • Experience managing products through the full development lifecycle.
  • Strong analytical and strategic thinking skills.
  • Excellent communication and stakeholder management abilities.
  • Experience working with cross-functional teams in regulated environments.

Preferred

  • Experience with CPAP masks, sleep therapy devices, respiratory interfaces, or ventilator accessories.
  • Knowledge of sleep apnea therapy, respiratory care workflows, and patient adherence challenges.
  • Familiarity with FDA, ISO 13485, MDR, and medical device product development processes.
  • Experience in human factors engineering and user-centered design.
  • MBA or advanced degree in a related field.

Key Competencies

  • Product Strategy
  • Voice of Customer
  • Market Analysis
  • Medical Device Development
  • Clinical Understanding
  • Human Factors & Usability
  • Cross-Functional Leadership
  • Commercialization
  • Data-Driven Decision Making
  • Regulatory Awareness

Success Metrics

  • Achievement of product revenue and profitability targets.
  • Successful launch of new CPAP and respiratory mask products.
  • Improved patient comfort, fit, and therapy adherence metrics.
  • Market share growth within sleep and respiratory care segments.
  • On-time and on-budget execution of development projects.
  • Customer satisfaction and Net Promoter Score (NPS) improvements.

Ideal Candidate Profile

A successful candidate combines the strategic mindset of a product leader with a deep understanding of patient needs in sleep and respiratory therapy. They are passionate about improving therapy adherence, patient comfort, and clinical outcomes through innovative mask and interface solutions while navigating the complexities of the medical device industry.