V

Verathon

Bladder measurement and airway visualization devices

Design Quality Engineer 2

Biomedical Engineering & Medical Devices +1Confirmed live in the last 24 hours
Full-timeBurnaby, BC, Canada

About the Job

Requirements

  • A Bachelor's degree in Engineering, specifically Mechanical, Electrical, Biomedical, or a related field; a Master's degree is a plus.
  • Professional Engineer (P.Eng) or Engineer-in-Training (EIT) eligibility is required.
  • At least 3 years of experience in quality engineering, particularly in medical devices or related fields.
  • Familiarity with design control processes, risk management methodologies, and quality management systems.
  • Knowledge of relevant regulatory standards, including ISO, IEC, and FDA standards.
  • Proficiency in statistical analysis.
  • Verbal and written communication skills to collaborate effectively with cross-functional teams.

Responsibilities

  • Develop and implement quality plans, risk management strategies, risk management reports, system risk assessments, software risk assessments, and cybersecurity risk assessments.
  • Review and approve validation protocols and reports for design verification and validation activities, including IQ, OQ, and PQ.
  • Partner with product development engineering and core teams to identify, communicate, and execute design control and risk management deliverables across multiple projects.
  • Define compliance testing requirements aligned with national and international quality and conformity standards.
  • Collaborate with systems and design engineering teams to create, maintain, and enhance uFMEAs and dFMEAs.
  • Support new product development, lead design transfer to manufacturing, and support sustaining engineering throughout the product lifecycle.
  • Improve the Quality Management System and quality assurance processes to ensure compliance with Canadian and international standards.
  • Lead product failure investigations and corrective and preventive action initiatives.
  • Produce compliant risk reports, verification and validation test reports, statistical analyses of experimental and quality data, receiving inspection requirements, and post-market surveillance plans.
  • Establish and refine product cybersecurity protocols and security risk assessments in collaboration with the software development team.
  • Design and conduct experiments to assess component and supplier process reliability.

Desired Qualifications

  • A Master's degree is a plus.
  • Relevant certifications, such as CQE or CQA, are a plus.

About the Company

Verathon

Bladder measurement and airway visualization devices

Verathon makes medical devices that help clinicians care for patients more safely. Its main products are BladderScan, a noninvasive ultrasound device that estimates bladder volume to prevent unnecessary catheterizations, and the GlideScope video laryngoscope, which provides a clear view of the airway to improve intubation success. These tools rely on ultrasound imaging and video visualization to guide clinical decisions without invasive insertion when possible. The company differentiates itself with a focused line of reliable airway- and bladder-management devices and a global presence, aiming to improve patient care and broaden access to its products.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Bothell, WA
Founded
1984

Recently Posted Jobs

Explore more opportunities at Verathon

See more jobs