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Research And Development Engineer Medical Device Jobs in Seattle, WA

Socket.dev

Sales Solutions Engineer

Woodinville, WA · On-site

$120 - $180/hr

... R&D, influencing future repair capabilities, device priorities, and product roadmap decisions ... Familiarity with capital medical equipment including ultrasound, patient monitoring, anesthesia ...

1 point system

Systems Engineer III

Bellevue, WA · On-site

... R&D team at our Bellevue office. In this role, you will be responsible for driving the ... development and integration of complex, end-to-end medical device systems that involve wearable ...

Verathon, Inc.

Mechanical Engineer II

Bothell, WA

$96K - $118K/yr

... development of medical device components and subsystems. This includes contributing to the ... For more information, please visit our complete Benefits Summary at Research shows that women and ...

Verathon, Inc.

Mechanical Engineer II

Bothell, WA · On-site

$96K - $118K/yr

... R&D team located in Bothell, WA. This role is expected to work primarily on-site at our Bothell ... development of medical device components and subsystems. This includes contributing to the ...

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All JobsResearch And Development Engineer Medical Device JobsResearch And Development Engineer Medical Device Jobs in Seattle, WA

Research And Development Engineer Medical Device information

See Seattle, WA salary details

$22.8K

$109.9K

$171.8K

How much do research and development engineer medical device jobs pay per year?

As of Aug 24, 2026, the average yearly pay for research and development engineer medical device in Seattle, WA is $109,900.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,200.00 and $133,100.00 per year, depending on experience, location, and employer.

What does a research and development engineer do in the medical device industry?

A Research and Development (R&D) Engineer in the medical device industry is responsible for designing, developing, and testing new medical devices and technologies. They work closely with cross-functional teams to ensure products meet regulatory standards, are safe for patient use, and address clinical needs. Their tasks may include prototyping, conducting experiments, analyzing data, and collaborating with manufacturing teams to bring products from concept to market. R&D Engineers also stay updated on technological advancements and regulatory changes to ensure innovation and compliance.

What are the key skills and qualifications needed to thrive as a research and development engineer in the medical device industry?

To excel as a Research and Development Engineer in Medical Devices, you need a solid background in biomedical engineering or a related field, strong problem-solving skills, and experience with product development cycles. Familiarity with CAD software, prototyping tools, regulatory standards like ISO 13485, and relevant certifications (such as Six Sigma) is highly valued. Excellent teamwork, creativity, and effective communication are crucial soft skills for collaborating across multidisciplinary teams and driving innovation. These competencies ensure the design and launch of safe, effective, and compliant medical devices that improve patient outcomes.

What are some common challenges faced by research and development engineers in the medical device industry?

Research and Development Engineers in the medical device industry often face challenges such as navigating complex regulatory requirements, managing tight project timelines while ensuring product safety and efficacy, and collaborating with cross-functional teams like quality assurance and clinical affairs. Additionally, adapting to rapid technological advancements and integrating feedback from clinicians and end-users into the design process can be demanding. These challenges require strong problem-solving skills, adaptability, and effective communication to deliver innovative and compliant medical devices.

What is the difference between Research And Development Engineer Medical Device vs Quality Assurance Engineer Medical Device?

AspectResearch And Development Engineer Medical DeviceQuality Assurance Engineer Medical Device
Primary FocusDesigning, developing, and testing new medical device productsEnsuring products meet quality standards and regulatory requirements
Required CredentialsEngineering degree, knowledge of product developmentEngineering or science degree, knowledge of quality systems
Work EnvironmentResearch labs, product development teamsManufacturing facilities, quality control departments
Industry UsageInvolved in innovation and product creationInvolved in compliance, validation, and process improvement

While both roles require engineering knowledge and are integral to the medical device industry, Research And Development Engineers focus on creating and testing new products, whereas Quality Assurance Engineers ensure these products meet safety and quality standards throughout production.

What are popular job titles related to Research And Development Engineer Medical Device jobs in Seattle, WA?

For Research And Development Engineer Medical Device jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Research And Development Engineer Medical Device jobs in Seattle, WA look for?

The top searched job categories for Research And Development Engineer Medical Device jobs in Seattle, WA are:

Research And Development Engineer Medical Device jobs near you

Design Quality Engineer - Medical Devices & Regulatory Compliance

Tech Mirrors

Bothell, WA • On-site

Other

Posted 6 days ago

Job description

Job Title:Design Quality Engineer – Medical Devices
Location:Bothell, WA
Work Mode:Onsite
Client:Tata Elxsi | Philips

Job SummaryWe are looking for a Design Quality Engineer (DQE) with experience in medical devices and FDA-regulated environments. The role involves supporting product quality throughout the design and development lifecycle, ensuring compliance with regulatory and quality standards.

Key ResponsibilitiesSupport Design Control activities as per FDA and ISO standards
Participate in design reviews, verification, and validation activities
Review design documents, technical files, and change requests (ECR/ECO)
Maintain traceability documentation including DHF, DMR, and DHR
Support design transfer activities to manufacturing
Drive Risk Management activities including FMEA and hazard analysis
Ensure implementation and documentation of risk controls
Support CAPA activities, root cause analysis, and audit readiness
Work closely with cross-functional teams including R&D, Manufacturing, and Regulatory
Required Skills & Experience5+ years of experience in FDA-regulated medical device environments
Strong knowledge of Design Control and Design Assurance processes
Experience with Risk Management and Design for Reliability
Familiarity with:21 CFR Part 820
ISO 13485
ISO 14971
EU MDR and other medical device regulations
Experience with change management and manufacturing transfer
EducationBachelor’s Degree in Medical Sciences, Healthcare Management, Industrial Engineering, Supply Chain Management, or related field.

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