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Mechanical Engineer

  • Burnaby, BC, Canada

$81,940 to $95,674 CAD / year · Full-time

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Job details

Pay
$81,940 to $95,674 CAD / year
Job type
Full-time
Apply by
Posting language
English
Posted

Original job description

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. Two areas where Verathon has significantly impacted patient care, and become the market leader in each, are bladder volume measurement and airway management. The company’s BladderScan portable ultrasound and GlideScope video laryngoscopy & bronchoscopy systems effectively address unmet needs for healthcare providers and meaningfully raise the standard of care for patients. Verathon, a subsidiary of Roper Technologies, is headquartered in Bothell, Washington, USA and has international subsidiaries in Canada, Europe and Asia Pacific. For more information, please visit www.verathon.com.

Overview

Verathon® is looking for a Mechanical Engineer II to become the newest member of our Airway Sustaining Team located in Burnaby, British Columbia.

The Mechanical Engineer II is responsible for interacting with design and manufacturing resources to create changes for manufacturability, reliability, and cost effectiveness.

Responsibilities

  • Participate in designing, prototyping, testing and qualification of mechanical designs for high-reliability and high-performance medical devices.
  • Complete root cause investigations of manufacturing and design related failures and recommend solutions.
  • Support production activities and resolve issues quickly.
  • Evaluate product non-conformances and recommend design modifications.
  • Develop and test new manufacturing processes.
  • Review vendors process validation plans/protocols.
  • Creating test plans to verify solutions.
  • Act as a liaison between the design and manufacturing groups.
  • Assessing risk of solutions and updating technical risk documentation.
  • Work closely with electrical and software engineers, designing with system-wide perspective.
  • Interact with global and internal design and manufacturing resources to design for manufacturability, reliability and cost-effectiveness.
  • Specify and manage tool development.
  • Follow all policies, procedures and standards for engineering documentation to ensure compliance with corporate document management policy.

Qualifications

  • Bachelor and / or graduate degree in Mechanical Engineering
  • 2+ years of technical product or mechanical device design and manufacturing
  • Proven background of reviewing or preparing process validations.
  • Good knowledge of and ability to use SolidWorks and SolidWorks add-ins.
  • Experience using statistical techniques, preferably using Minitab.
  • A history of accurately identifying and documenting root cause.
  • Experience in technical team-focused workplace.
  • Ability to make independent judgments using sound engineering principles and techniques.
  • Proficient in writing concisely and accurately with meticulous attention to detail and clarity.
  • EIT status preferred

Why Join Us?

  • Be part of an innovative team that is dedicated to improving patient outcomes.
  • Engage in meaningful work that makes a difference in the healthcare industry.
  • Competitive salary and comprehensive benefits package.
  • Salary range - $81,940 - $95,674 (Compensation will vary based on skills, experience and location; it is not typical to be hired at or above the top of the salary range).
  • Full-time employees who are not on a commission plan are eligible for Verathon’s annual bonus plan based on company and individual performance.
  • Verathon provides a competitive benefits package including a generous HCSA, paid holidays, paid time off and a retirement matching plan.
More about this job

Responsibilities

Design, prototype, test, and qualify mechanical designs for medical devices, while investigating failures, resolving production issues, and recommending design or process improvements. Collaborate with design, manufacturing, electrical, and software teams to improve manufacturability, reliability, and cost-effectiveness, and maintain risk and engineering documentation.

Requirements

A bachelor’s or graduate degree in Mechanical Engineering and at least two years of experience in technical product or mechanical device design and manufacturing are required. Candidates should have experience with process validation, SolidWorks, statistical techniques such as Minitab, root cause analysis, and clear technical writing; EIT status is preferred.

Skills

  • Mechanical Design
  • Prototyping
  • Testing
  • Root Cause Analysis
  • Manufacturing Support
  • Process Validation
  • Design for Manufacturability
  • Reliability Engineering
  • Risk Assessment
  • SolidWorks
  • Minitab
  • Statistical Techniques
  • Technical Documentation
  • Tool Development
  • Cross-Functional Collaboration

Benefits

  • Health Care Spending Account
  • Paid Holidays
  • Paid Time Off
  • Retirement Matching Plan
  • Annual Bonus Plan

Visa sponsorship

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Categories

  • Engineering
  • Manufacturing
  • Healthcare

Keywords

  • Mechanical Engineering
  • Medical Devices
  • BladderScan
  • GlideScope
  • Airway Management
  • Mechanical Design
  • Prototyping
  • Design Qualification
  • Root Cause Investigation
  • Manufacturing
  • Process Validation
  • Non-Conformance Evaluation
  • Manufacturing Process Development
  • Test Plans
  • Risk Documentation
  • Design for Manufacturability
  • Reliability
  • Cost-Effectiveness
  • Tool Development
  • SolidWorks
  • SolidWorks Add-Ins
  • Minitab
  • Statistical Techniques
  • Engineering Documentation
  • EIT

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