Elevate quality assurance in manufacturing with Sonova as a Manufacturing Engineering QA Manager. You'll ensure compliance with MDSAP and MDR, and lead key quality initiatives. In this senior role based in Kitchener, Canada, you will oversee QA processes while collaborating closely with Manufacturing Engineering and Global Services teams.

The position emphasizes design transfer, process validation, and compliance with international regulations such as ISO 13485 and MDR. Your analytical skills will be critical as you manage performance indicators and implement quality improvements. Key Responsibilities:

- Maintain QA document control for compliance
- Collaborate on design transfer and process validation
- Support internal and external audit preparations
- Analyze OPS Key Performance Indicators for improvements
- Coordinate CAPA and handle nonconforming product resolutions

Requirements:

- Graduate degree in engineering or relevant field
- 4+ years in medical device quality roles
- Knowledge of ISO 13485, ISO 9001, and MDR
- Solid communication and problem-solving skills
- Advanced MS Office skills required

Lead QA excellence and enhance operational quality metrics at Sonova in Kitchener.

📌 QA Manager in Manufacturing Engineering at Sonova (Waterloo)
🏢 Sonova Group
📍 Waterloo