Lead the way in quality assurance with Sonova as a Manufacturing Engineering QA Manager. Drive compliance and operational excellence in a role that champions creative hearing solutions.
Join Sonova’s team to oversee comprehensive QA processes within manufacturing engineering for medical devices. This critical position requires expertise in design transfer, process validation, and regulatory compliance, specifically MDSAP and MDR. You'll ensure high operational quality metrics while collaborating with various teams in a dynamic, hybrid work environment.
Key Responsibilities:
• Maintain QA activities and monitor compliance with regulations
• Support alignment with ISO standards and regulatory requirements
• Collaborate on design transfer and process validation activities




• Prepare for internal and external audits and CAPA closure
• Trend OPS Key Performance Indicators to suggest quality improvements
Requirements:
• Graduate degree in engineering, science, or a related field
• 4+ years in medical device manufacturing quality roles
• Knowledge of ISO 13485, ISO 9001, and MDR regulations
• Strong communication and problem-solving skills
• Advanced MS Office proficiency, with SAP experience preferred
Make an impact on hearing health with your QA expertise at Sonova.
#J-18808-Ljbffr

📌 Quality Assurance Manager at Sonova (Kitchener)
🏢 Sonova Group
📍 Kitchener