Senior Quality Design Assurance Engineer

at  Boston Scientific Corporation

Montréal, QC, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate16 Feb, 2025Not Specified17 Nov, 20247 year(s) or aboveRegulated Industry,Presentation Skills,Biomedical EngineeringNoNo
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Description:

REQUIRED QUALIFICATIONS:

  • Bachelor’s degree in mechanical, electrical, or biomedical engineering, or equivalent.
  • 7+ years of work experience relating to quality assurance in a highly regulated industry.
  • Medical device experience
  • Competent with use of Microsoft Office Suite

PREFERRED QUALIFICATIONS

  • Focus on detailed work with emphasis on accuracy and completeness
  • Excellent organizational and planning skills; drives for results
  • Strong communication (oral and written) and presentation skills
  • High energy problem solver capable of driving items to closure
  • Ability to collaborate and work on a global team

How To Apply:

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Responsibilities:

ABOUT THE ROLE

The ideal Senior Design Quality Assurance Engineer will bring their leadership to new product development projects and sustaining projects for our innovative cardiovascular products. Furthermore, they will develop, establish, and maintain quality-engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements.

YOUR RESPONSIBILITIES WILL INCLUDE:

  • Develops understanding of Design Controls, Risk Management and Usability for Medical Devices.
  • Provide quality and compliance input to project teams for project decisions and deliverables (i.e., Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Reviews, Design V&V, Usability Testing, SW Validation, Process Validation and Labeling).
  • Provide quality and compliance input for post market product sustaining activities, such as design changes, NCEP’s, CAPA’s PIRs, Field Signals Evaluations and Field Actions.
  • Applies technical skills including sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
  • Responsible for collaborating within a team to identify and implement effective controls to support development or maintenance of products to meet internal and external requirements.
  • Builds quality into all aspects of work by maintaining compliance to all quality requirements.
  • Support internal and external regulatory audits as required.
  • Other duties as necessary or required by the organization.


REQUIREMENT SUMMARY

Min:7.0Max:12.0 year(s)

Pharmaceuticals

IT Software - Other

Clinical Pharmacy

Graduate

Mechanical electrical or biomedical engineering or equivalent

Proficient

1

Montréal, QC, Canada