ZipRecruiter

Log In

1

Seasonal Biomedical Design Engineer Jobs in Renton, WA

Amazon

Mechanical Design Engineer, AFT Quality

Bellevue, WA · On-site

$85K - $116K/yr

... as seasonal or temporary employment. The benefits that generally apply to regular, full-time ... practices for part design, and advanced assemblies - 8+ years of engineering experience ...

next page

Showing results 1-20

All JobsBiomedical Design Engineer JobsSeasonal Biomedical Design Engineer JobsSeasonal Biomedical Design Engineer Jobs in Renton, WA

Seasonal Biomedical Design Engineer information

See Renton, WA salary details

$46.1K

$106.6K

$157.5K

How much do seasonal biomedical design engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for seasonal biomedical design engineer in Renton, WA is $106,641.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,800.00 and $130,500.00 per year, depending on experience, location, and employer.

What is the difference between Seasonal Biomedical Design Engineer vs Biomedical Equipment Technician?

AspectSeasonal Biomedical Design EngineerBiomedical Equipment Technician
CredentialsBachelor's in Biomedical Engineering or related fieldAssociate's or Bachelor's in Biomedical Technology or related field
Work EnvironmentDesign labs, research facilities, product developmentHospitals, clinics, maintenance workshops
Employer & IndustryMedical device companies, research institutionsHospitals, healthcare providers, service companies

The Seasonal Biomedical Design Engineer focuses on designing and developing new biomedical devices, often working in labs or research settings. In contrast, the Biomedical Equipment Technician primarily maintains, repairs, and calibrates existing medical equipment in healthcare facilities. Both roles require technical knowledge but differ in their focus on design versus maintenance.

Is there a high demand for seasonal biomedical design engineers?

The demand for seasonal biomedical design engineers varies with industry needs and project cycles, often peaking during product development or medical device launches. While full-time roles are more common, some companies hire temporary or contract engineers for specific projects, especially in research and development environments that require specialized skills in CAD software and regulatory compliance.
Seasonal Biomedical Design Engineer jobs near you

Design Engineer (Medical Device)

S-Solutions Inc- a SyeDyn Company

Bothell, WA • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Design Quality Engineer

Work location: USA (Bothell/Cambridge)


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


    Apply