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Biomedical Design Engineer Jobs in Seattle, WA (NOW HIRING)

Anagha Techno Soft

Design Quality Engineer

Bothell, WA · On-site

Design Quality Engineer Work location: Bothell/Cambridge, WA (Onsite) Client : Tata Elxsi The ... Bachelor's Degree in Medical Sciences, Healthcare Management, Biomedical Engg Minimum required ...

New

DeepSight Technology

Image Analysis Engineer

Seattle, WA · On-site

$160K - $250K/yr

M.S. in Electrical/Biomedical Engineering* 7+ years industry experience in medical imaging product development* Expertise in ultrasound physics and system design, signal and image processing ...

DeepSight Technology

Image Analysis Engineer

Seattle, WA · On-site

$160K - $250K/yr

S. in Electrical/Biomedical Engineering • 7+ years industry experience in medical imaging product development • Expertise in ultrasound physics and system design, signal and image processing ...

Crowdstaffing

Mechanical Engineer III

Bothell, WA

... design FMEA that feeds into the module design FMEAs. [4] Setting up the database that is used by ... Minimum Qualifications [1] Bachelors or Master's Degree in Mechanical / Electrical / Biomedical ...

Danaher

Software Engineer Internships

Tacoma, WA · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Software Engineering, Biomedical Engineering (with computational focus), or related field

Danaher

Software Engineer Internships

Seattle, WA · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Software Engineering, Biomedical Engineering (with computational focus), or related field

Danaher

Software Engineer Internships

Bellevue, WA · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Software Engineering, Biomedical Engineering (with computational focus), or related field

1 point system

Systems Engineer III

Bellevue, WA · On-site

Experience in developing system design verification and validation plans and functional test ... Bachelor's or Master's degree in Electrical Engineering, Biomedical Engineering, Computer ...

Infotech Sourcing

Acoustic Test Engineer

Kirkland, WA · On-site

... design controls). There will be close collaboration with a senior engineer who owns the test ... biomedical engineering, or a related technical field -- or equivalent hands-on lab/test experience ...

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Showing results 1-20

All JobsBiomedical Design Engineer JobsBiomedical Design Engineer Jobs in Seattle, WA

Biomedical Design Engineer information

See Seattle, WA salary details

$46.7K

$107.9K

$159.3K

How much do biomedical design engineer jobs pay per year?

As of Aug 16, 2026, the average yearly pay for biomedical design engineer in Seattle, WA is $107,891.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,800.00 and $132,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a biomedical design engineer?

To thrive as a Biomedical Design Engineer, you need a solid grounding in biomedical engineering principles, proficiency in CAD software, and typically a bachelor's or master’s degree in biomedical engineering or a related field. Familiarity with tools like SolidWorks or AutoCAD, regulatory standards (such as ISO 13485 or FDA guidelines), and experience with prototyping equipment are highly valued. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help you excel when collaborating with interdisciplinary teams. These attributes are vital for ensuring the safe, innovative, and effective design of medical devices and technologies.

What is a biomedical design engineer?

A Biomedical Design Engineer designs and develops medical devices, prosthetics, and healthcare technologies to improve patient care. They combine principles of engineering and biology to create innovative solutions for medical challenges. Their work includes designing prototypes, testing materials, ensuring regulatory compliance, and collaborating with medical professionals.

What does a biomedical design engineer do?

A typical day for a Biomedical Design Engineer involves developing and refining medical device designs, creating technical drawings and 3D models, and collaborating with cross-functional teams including clinicians, regulatory specialists, and manufacturing staff. You may spend time conducting prototype testing, troubleshooting design challenges, and documenting design changes to meet quality standards. Regular meetings are common to gather user feedback and ensure alignment with project goals. This hands-on, collaborative environment fosters both technical growth and meaningful contributions to healthcare innovation.

What are the most commonly searched types of Biomedical Design Engineer jobs in Seattle, WA?

The most popular types of Biomedical Design Engineer jobs in Seattle, WA are:

What are popular job titles related to Biomedical Design Engineer jobs in Seattle, WA?

For Biomedical Design Engineer jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Biomedical Design Engineer jobs in Seattle, WA look for?

The top searched job categories for Biomedical Design Engineer jobs in Seattle, WA are:

Biomedical Design Engineer jobs near you
Infographic showing various Biomedical Design Engineer job openings in Seattle, WA as of August 2026, with employment types broken down into 60% Full Time, and 40% Contract. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $107,891 per year, or $51.9 per hour.

Design Quality Engineer

Anagha Techno Soft

Bothell, WA • On-site

Other

Posted 2 days ago

New

Job description

Title : Role: Design Quality Engineer
Work location: Bothell/Cambridge, WA (Onsite)
Client : Tata Elxsi
The Design Quality Engineer (DQE) is responsible for ensuring that products are designed and developed in compliance with regulatory standards, quality requirements, and customer expectations. This role works closely with R&D, regulatory, manufacturing, and suppliers to embed quality into product design.
Design Control
  • Ensure compliance with Design Control requirements (21 CFR Part 820 / ISO 13485) throughout product lifecycle
  • Participate in design planning, design reviews, and design verification/validation activities. (cross-functional design reviews, ensuring closure of action items)
  • Review and approve design inputs, outputs, and technical documentation.
  • Support traceability matrix (DHF, DMR, DHR) creation and maintenance.
  • Ensure Design Verification & Validation (V&V) activities meet requirements
  • Review and approve, Engineering Change requests/Orders (ECR/ECOs).
  • Ensure design changes follow proper change control processes.
  • Builds and nurtures effective relationships with internal and external stakeholders, providing expert guidance and mentorship to cross-functional teams, ensuring alignment with quality standards and successful project milestones.
  • Validates critical design inputs such as usability, reliability, performance, manufacturability, and safety, ensuring alignment with both quality standards and regulatory requirements.
  • Design transfer to manufacturing, ensuring process readiness
Risk Management Support
  • Guide comprehensive risk management activities throughout the product lifecycle to ensure risks are identified and mitigated
  • Facilitate FMEA (Design and Process) and hazard analysis.
  • Ensure risk controls are implemented, verified, and documented.
QMS Support (Audit, CAPA)
  • Ensure preparation for quality audits and inspections, maintaining documentation to demonstrate compliance
  • Record, manage, and execute CAPA processes including root cause analysis and implementation of solutions
  • Contributes to the development, implementation, and revision of QMS processes
Minimum required Education:
Bachelor's Degree in Medical Sciences, Healthcare Management, Biomedical Engg
Minimum required Experience:
  • Knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts 820, ISO 13485, ISO 14971, European Medical Device Directive (93/42/EEC), EU Medical Device Regulation (EU MDR), Canadian Medical Devices Regulation (SOR/98-282), etc
  • Change Management (Including design and Manufacturing transfer)
  • Minimum of 5+ years experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of Risk
  • You have detailed experience in identifying, promoting, and supporting processes and design quality tools for use in tracking/preventing product defects, design traceability, and Design for Reliability

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