Top 12 Biomedical engineer Jobs in Seattle, Wa

Medical Device Design Controls & Remediation Engineer
Amaris Consulting —Bothell, WA
- English
- Mid-level
- 3 years
Ultrasound Engineer
United Imaging Healthcare North America, Inc. —Bellevue, WA
- Doctor of Philosophy
- Team management
- Travel
Clinical Engineer - Cardiac (Temporary)
Fujifilm —Bothell, WA
- $65 - $75 an hour
- Temporary
- 5 years
- Mid-level
- Office
Senior Clinical Engineer (onsite Bothell, WA)
Fujifilm —Bothell, WA
- $110,000 - $135,000 a year
- Office
- Microsoft Office
- 8 years
- Paid holidays
- Disability insurance
Image Analysis Engineer
DeepSight Technology —Seattle, WA
- $160,000 - $250,000 a year
- Full-time
- 7 years
- Office
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
Senior Systems Engineer
Verathon, Inc. —Bothell, WA
- $149,061 - $184,716 a year
- Full-time
- Bachelor of Science
- Engineering
- ERP systems
- Paid holidays
- Health insurance
Scientist/Senior Scientist, Protein Engineering
SystImmune —Redmond, WA
- $90,000 - $130,000 a year
- Full-time
- Doctor of Philosophy
- Ability to sit for extended periods
- Senior level
- Paid holidays
- Disability insurance
Managing Engineer, Biomechanics (Ph.D.)
Exponent Inc. —Seattle, WA
- $143,000 - $180,000 a year
- Email
- 6 years
- Office
- Doctor of Philosophy
- 401(k)
Lead Systems Engineer
Katalyst Healthcares & Life Sciences —Bothell, WA
- Call employer
- Master's degree
- Team management
- US work authorization
Quick Apply
Senior Product Engineer
Steris —Seattle, WA
- $90,737.50 - $117,425.00 a year
- Full-time
- Oracle
- Engineering
- Supervising experience

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Ultrasound Engineer
United Imaging Healthcare North America, Inc. —Bellevue, WA
You will develop software tools, image and data analytics infrastructure, and test methods to facilitate pre-clinical and clinical evaluation.

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biomedical engineer jobs near seattle, wa

Medical Device Design Controls & Remediation Engineer

Amaris Consulting -
Bothell, WA

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Job Details

Qualifications

Developing medical devices
Content creation for technical audiences
Requirements specification
Engineering development testing
Requirements design
Regulatory compliance
English
Quality risk management
Requirements analysis
Requirements management
Engineering product development
Design controls
Biomedical regulatory compliance
Technical writing experience within technology
Cross-functional collaboration
Test validation method
ISO 13485
Product design documentation
Cross-functional communication
FDA regulations

Full Job Description

We are looking for dynamic consultants to grow our Life Sciences team in Bothell, Washington. Your experience, knowledge, and commitment will help us to face our client's challenges.

You will be supporting different projects through your expertise as Medical Device Design Controls & Remediation Engineer.

Your main responsibilities:

Identify and remediate gaps between user needs, design requirements, risk analyses, and verification/validation evidence across multiple medical device product families.
Author and update design control documentation, including requirements specifications, DFMEA, PFMEA, UFMEA, Risk Management Matrices (RMM), and V&V protocols and reports.
Build and repair end-to-end requirements traceability from business, user, and regulatory requirements through verification evidence and product documentation.
Develop verification and validation test protocols where evidence is missing, ensuring compliance with FDA and ISO design control requirements.
Prepare and structure remediated documentation for migration from legacy systems (e.g., Windchill) into CodeBeamer or other ALM platforms.
Track remediation activities, documentation gaps, deliverables, and program metrics using Azure DevOps and communicate progress to program stakeholders.

Qualifications:

Bachelor’s or Master’s degree in Biomedical, Systems, Mechanical, Electrical Engineering, or a related engineering discipline.
3–7+ years of experience in medical device product development within a regulated design controls environment.
Strong hands-on experience with ISO 14971 risk management, including DFMEA, PFMEA, UFMEA, and Risk Management Matrix (RMM) activities.
Proven experience authoring verification and validation protocols, reports, requirements specifications, and traceability documentation.
Working knowledge of FDA Design Controls / 21 CFR 820.30, ISO 13485, and ALM/requirements management tools such as CodeBeamer, Polarion, IBM DOORS, or Windchill.
Excellent technical writing, analytical, organizational, and communication skills, with professional fluency in English and the ability to work effectively in a cross-functional hybrid environment.

Why choose us

An international community bringing together more than 110 different nationalities
An environment where trust is central: 70% of our leaders started their careers at the entry level
A strong training system with our internal Academy and more than 250 modules available
A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)

Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

#LI-JM1

Who are we?

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:

Brief Call: Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!

Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!

Case study: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.

As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.
We look forward to meeting you!

Apply Now

Refine Your Search

biomedical engineer jobs in seattle, wa

Medical Device Design Controls & Remediation Engineer

Ultrasound Engineer

Clinical Engineer - Cardiac (Temporary)

Senior Clinical Engineer (onsite Bothell, WA)

Image Analysis Engineer

Senior Systems Engineer

Scientist/Senior Scientist, Protein Engineering

Managing Engineer, Biomechanics (Ph.D.)

Lead Systems Engineer

Senior Product Engineer

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