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Kardium Inc.

Process Quality Engineering Team Lead – Operations

Kardium Inc.

. Develop a detailed understanding of Kardium’s products and manufacturing processes .

Posted 10/17/2026full-timeBurnaby • CanadaSenior💰 CA$102,000 - CA$120,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in leading quality engineering initiatives within a manufacturing environment, focusing on non-conformance management, root-cause analysis, and continuous improvement. Possesses strong communication skills to effectively collaborate with cross-functional teams and drive product quality enhancements.

Highest-signal resume keywords
Process Quality Engineering LeadershipNon-Conformance ManagementRoot-Cause AnalysisContinuous Improvement InitiativesMedical Device Industry Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Quality Engineering ToolsStatisticsSPCFMEAProcess CapabilityFailure InvestigationsProduct Quality MonitoringTechnical CommunicationManufacturing ProcessesEngineering Experience
Soft Skills
Interpersonal SkillsConsensus BuildingWritten CommunicationVerbal Communication
Certifications & Qualifications
Bachelor’s Degree in Science or Engineering
Industry Keywords
Medical DevicesRegulated IndustriesManufacturing EnvironmentCross-Functional PartnershipsQuality ControlQuality Assurance

About the role

Key responsibilities & impact
  • Develop a detailed understanding of Kardium’s products and manufacturing processes
  • Lead a team of Process Quality Engineers in a fast-paced manufacturing environment
  • Triage, prioritize, and schedule operational and project work
  • Lead investigations with engineering subject matter experts
  • Review and disposition non-conforming products and materials
  • Lead NC disposition and rework activities for Catheter/Introducer subassembly processes
  • Support and drive continuous improvement initiatives
  • Investigate systemic product quality issues
  • Build and maintain cross-functional partnerships with Quality Control, Engineering, Manufacturing, and Quality Assurance
  • Design, implement, and improve processes for monitoring, evaluating, and reporting product quality trends and process performance
  • Act as the primary point of contact for production quality concerns across a two-shift operation

Requirements

What you’ll need
  • Bachelor’s degree or higher in science or engineering
  • Mechanical engineering background preferred
  • At least 8 years of engineering experience in a technical, multi-disciplinary environment
  • Experience with medical devices or similarly regulated industries highly advantageous
  • Excellent interpersonal skills and track record of driving consensus with diverse stakeholders
  • Excellent written and verbal communication skills, especially in a technical context
  • Proven experience with non-conformances, failure investigations, root-cause analysis, and quality engineering tools
  • Sound knowledge of statistics, SPC, FMEA, process capability, and related concepts

Benefits

Comp & perks
  • 5% RRSP contribution
  • Stock option plan for permanent employees
  • Comprehensive medical and dental coverage effective Day 1, with no waiting period
  • 3 personal days per year
  • Well-being support for employees and dependents
  • Career progression and learning support
  • Professional membership support
  • Maternity leave top-up
  • Adoptive leave top-up
  • Benefit coverage for fertility drug treatment
  • Work-day flexibility
  • Employee Resource Groups and inclusion support