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OrthoPediatrics

Quality Intern

Laval, QC, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Nov 26, 2026
Posting language: English
Posted: Oct 27, 2026

Original job description

Position Overview

The Quality intern supports product development, manufacturing, quality assurance, and regulatory compliance activities for medical devices. This role is responsible for managing design changes, maintaining technical and quality documentation, supporting supplier and manufacturing quality, ensuring compliance with ISO 13485 and regulatory requirements, and contributing to continuous improvement initiatives.

Key Responsibilities

Implement design changes, DFM activities, and product improvements.
Create, update, and maintain inspection and manufacturing documentation.
Manage non-conforming products, supplier rework activities, and corrective actions.
Support process validation, equipment maintenance, and manufacturing quality activities.
Maintain technical and regulatory documentation, including DHF, DMR, and MDR files.
Support the Quality Management System (QMS) and ensure compliance with ISO 13485 and applicable regulations.
Assist with complaint handling, investigations, CAPA, and non-conformance evaluations.
Prepare regulatory submissions and responses to international regulatory authorities.
Support internal and external audits and provide required documentation.
Participate in continuous improvement projects and process enhancement initiatives.
Coordinate prototype manufacturing activities and supplier follow-up.
Assist with product release documentation and market launch approvals.

Required Qualifications

· Mechanical or Biomechanical Engineers
· Detail-oriented and strong organizational, problem solving and analytical skills
· Proficient in Microsoft Office Software
· Must be proficient in spoken/written English
· Must be eligible to work in Canada at time of application
· Must be enrolled as a full-time student in a Canadian University
· Knowledge of machining & manufacturing processes
Preferred Qualifications
· Knowledge of inspection equipment
· Regulatory or Quality System experience preferred
· Knowledge in 3D modeling and 2D drawings - SolidWorks experience preferred

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More about this job

Responsibilities

Support medical device product development, manufacturing quality, and regulatory compliance by managing design changes, maintaining technical and quality records, and assisting with supplier and manufacturing activities. Contribute to complaint investigations, CAPA, audits, regulatory submissions, product releases, and continuous improvement initiatives.

Requirements

Applicants must be mechanical or biomechanical engineering students enrolled full-time at a Canadian university and eligible to work in Canada. They should have strong organizational, analytical, and problem-solving skills, proficiency in Microsoft Office and English, and knowledge of machining and manufacturing; inspection equipment, quality systems, regulatory experience, and SolidWorks are preferred.

Skills

Design Change Management
Design for Manufacturing
Manufacturing Documentation
Inspection Documentation
Non-Conformance Management
Supplier Quality
Corrective Actions
Process Validation
Quality Management Systems
ISO 13485 Compliance
Regulatory Documentation
Complaint Handling
CAPA
Audit Support
Continuous Improvement
SolidWorks

Visa sponsorship

Not detected in the job text

Keywords

Medical Devices
ISO 13485
Quality Management System
Design History File
Device Master Record
Medical Device Reporting
Design Changes
Design for Manufacturing
Product Improvement
Manufacturing Processes
Machining
Inspection Equipment
Supplier Quality
Non-Conforming Products
Corrective Actions
Process Validation
Equipment Maintenance
Regulatory Compliance
Regulatory Submissions
Complaint Handling
Investigations
CAPA
Audits
Continuous Improvement
Prototype Manufacturing
Product Release
Microsoft Office
SolidWorks
3D Modeling
2D Drawings

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