Quality Engineer

About Savaria

Enhance patient mobility with Savaria as a Quality Engineer for Class I medical devices in Magog, Quebec. This role focuses on ensuring high-quality standards and continuous improvement in a 12–18 month assignment.

Savaria is seeking a dedicated Quality Engineer to join their Patient Care division at the Magog manufacturing site. This role demands strong collaboration with engineering and manufacturing teams to maintain the Quality Management System. You will oversee QA inspections and audits, helping to drive actionable improvements and ensure products meet regulatory requirements.

Key Responsibilities

• Collaborate with teams on product quality specifications
• Supervise QA Inspectors for device acceptance
• Administer audits program for quality compliance
• Maintain QA files and document control
• Coordinate equipment calibration and training

Requirements

• Bilingual in English and French
• 5+ years in Quality Engineering or Medical Device Regulatory
• Experience in the medical device industry preferred
• Skilled in statistical and root cause analysis
• Strong understanding of ISO 13485 and regulatory processes

Support health innovation through quality engineering practices at Savaria.