Validation and Verification Specialist

Montréal, Québec

On-site

Full-time

No salary posted1 weeks ago

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Employment type: Full-time · On-site
Posted: September 27, 2026
Province: Quebec (QC)

Hiring confidence: Sparse posting · 11/100

This posting is missing most of the signals we look for, or shows patterns common to listings that are not actively being filled. Check with the employer before applying. How this is scored

Job Overview

Jobs

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Join the Team! Joining Puzzle Medical means becoming part of a team dedicated to improving the treatment of advanced heart failure. You’ll contribute to the development of innovative technology designed to enhance patients’ quality of life and clinical outcomes. We offer a collaborative and dynamic MedTech environment where initiative is encouraged and ideas are valued. As a growing company, your work will have real impact and visibility, and you’ll have the opportunity to grow alongside the or…

This role is based in Quebec. Puzzle Medical Devices is hiring for this full-time position through Jobily, where you can check how well your resume matches the posting before you apply.

Market context

About this role in Quebec

Average salary for Validation and Verification Specialist in Quebec

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NOC code

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Typical qualifications for Canadian employers

Medical device or pharmaceutical industry experience preferred
Knowledge of validation and verification methodologies
Understanding of regulatory requirements (FDA, ISO standards)
Strong attention to detail
Technical documentation skills

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What you'll do

Conduct validation and verification testing of medical devices
Develop and execute test plans and protocols
Document testing results and maintain compliance records
Support product development lifecycle
Collaborate with cross-functional teams
Ensure adherence to regulatory standards and quality requirements
Contribute to process improvements

What you'll need

Medical device or pharmaceutical industry experience preferred
Knowledge of validation and verification methodologies
Understanding of regulatory requirements (FDA, ISO standards)
Strong attention to detail
Technical documentation skills
Problem-solving abilities