Full-time

Quality Assurance Specialist

Posted by Puzzle Medical Devices • June 09, 2026

📍 montreal (administrative region), qc, Canada
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Description

Position Summary

The Quality Assurance Specialist is responsible for reviewing and ensuring the completeness, accuracy, traceability, and compliance of manufacturing and production quality control documentation throughout the product lifecycle—from incoming inspection to final batch release.

This role plays a key part in maintaining product quality and regulatory compliance by reviewing Job Travelers, Device History Records (DHRs), inspection records, manufacturing documentation, metrology reports, machine shop documentation, and cleanroom records.

The ideal candidate is highly detail-oriented, rigorous, organized, and comfortable working in a fast-paced, cross-functional environment. Experience in highly regulated or precision-driven industries such as medical devices, automotive, aerospace, or aeronautics is highly valued.

Responsibilities

Documentation Review & Batch Record Review

  • Review and approve manufacturin...

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