Elevate your career at Puzzle Medical Devices® Inc. as a Quality Specialist in Montreal. This full time, in-person role focuses on ensuring high standards in medical device manufacturing and validation. In this critical position, you will support the development and compliance of a percutaneous heart pump system.

As a Quality Specialist, your responsibilities include managing supplier quality, guiding compliance with ISO 13485 standards, and participating in regulatory inspections. You will actively engage with cross-functional teams to maintain high-quality production standards. Key Responsibilities:

- Qualify and manage suppliers per regulatory standards
- Review supplier documentation and certifications
- Support quality investigations and nonconformance resolutions




- Execute software validation activities and maintain documentation
- Collaborate with R&D;, manufacturing, and regulatory teams Requirements:
- Bachelor’s degree in Mechanical, Biomedical, or related field
- Experience in a regulated medical device environment
- Knowledge of ISO 13485 and FDA QMSR
- Strong analytical mindset and organizational skills
- Excellent communication in cross-functional settings Bring your quality assurance expertise to help shape innovative medical solutions with Puzzle Medical Devices® Inc.

📌 Full-Time Quality Specialist in Montreal
🏢 Puzzle Medical Devices
📍 Montreal