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Manager, Design Quality Engineering

Job in Edmonton, Alberta, Canada
Listing for: Penta Search Group
Full Time position
Listed on 2026-06-03
Job specializations:
  • Engineering
    Regulatory Compliance Specialist, Product Engineer
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Job Description & How to Apply Below

A growing and globally active healthcare technology company is looking to add a Design Quality Engineering Manager to its team. This role will take ownership of quality leadership across product development programs, ensuring that new technologies are developed, validated, and launched in line with rigorous regulatory and performance standards.

About the Role

This position sits at the center of product innovation, partnering closely with engineering, regulatory, and operations teams to embed quality into every stage of development.

You’ll lead a small team while also acting as a key advisor on product quality, risk, and compliance—helping guide decisions that directly impact product success and patient outcomes.

Key Responsibilities
  • Provide leadership and direction to a team supporting quality activities within product development
  • Act as a core contributor on development teams, ensuring quality considerations are integrated from early design through commercialization
  • Oversee and evolve processes related to design assurance, risk evaluation, and product verification/validation
  • Ensure development activities align with applicable regulatory expectations across key global markets
  • Partner cross-functionally to address technical challenges and drive effective resolution of quality-related issues
  • Strengthen and refine internal processes to improve efficiency, compliance, and scalability
  • Support audit readiness and participate in regulatory inspections as needed
  • Contribute to planning efforts including team resourcing and operational priorities
Qualifications & Experience
  • Degree in Engineering, Science, or a related technical discipline (advanced degree considered an asset)
  • Several years of experience in quality, product development, or design assurance within a regulated environment
  • Prior experience leading or mentoring team members
  • Strong familiarity with regulatory frameworks governing medical or healthcare products (e.g., FDA, ISO, EU regulations)
  • Experience applying risk management principles and supporting design/development lifecycle activities
  • Exposure to areas such as electrical medical systems, connected devices, or sterile products is advantageous
  • Ability to influence across functions and communicate effectively with both technical and non-technical stakeholders
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