Release engineer Jobs in Coquitlam, BC

Company Overview

Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility. The company has significantly impacted patient care in bladder volume measurement and airway management, becoming the market leader in each area. Its BladderScan portable ultrasound and GlideScope video laryngoscopy & bronchoscopy systems address unmet needs for healthcare providers and raise the standard of care. Verathon, a subsidiary of Roper Technologies, is headquartered in Bothell, Washington, USA, with international subsidiaries in Canada, Europe, and Asia Pacific. For more information, please visit www.verathon.com.

Overview

The Mechanical Engineer III is responsible for designing and developing robust and innovative medical devices and equipment to support the commercialization of company-developed products. Responsibilities include cost estimation, design, verification, and validation. The engineer will collaborate with partners to deliver designs of electromechanical assemblies.

Responsibilities

• Work with vendors to complete designs
• Review vendor-provided designs to ensure they meet product requirements
• Research design options and perform experiments to assess feasibility
• Complete high-level design; work with external partners on detailed design
• Collaborate closely with electrical and software engineers, designing with a system-wide perspective
• Interact with global and internal design and manufacturing resources to optimize for manufacturability, reliability, and cost-effectiveness
• Create and release product requirements, design specifications, and descriptions in compliance with medical device standards and internal procedures
• Ensure engineering documentation complies with corporate policies
• Review product documentation for accuracy, including customer-facing materials
• Participate in designing, prototyping, testing, and qualifying high-reliability medical devices
• Support risk assessments, design reviews, pre-production, testing, and regulatory submissions
• Evaluate product non-conformances and recommend design modifications using analytical techniques
• Assist in the development of intellectual property

Qualifications

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