Join Sonova as a Manufacturing Engineering QA Lead, spearheading quality initiatives and ensuring MDSAP and MDR compliance in Kitchener, Canada. Your expertise will drive operational excellence.

This hands-on role requires leadership and extensive knowledge in the medical device sector, emphasizing design transfer, FMEA, and quality assurance projects. Collaborate with teams to support process validation while ensuring adherence to ISO standards and managing audit evidence collection. Your proactive approach in handling CAPA and nonconforming products will enhance the reliability of our systems and processes.

Key Responsibilities:



• Oversee QA activities for regulatory compliance • Support collaboration for design and validation tasks • Prepare for audits and manage CAPA processes • Trend analysis of quality metrics for improvements • Coordinate quality resolutions for nonconforming products

Requirements: • Master's degree in engineering or quality field • Minimum 4 years of quality experience in medical devices • Proficiency in ISO standards and regulatory guidelines • Solid problem-solving and stakeholder management skills • Proficient in MS Office and eQMS platforms

Drive quality assurance excellence at Sonova and make a significant impact on operational metrics. #J-18808-Ljbffr

📌 Sonova Manufacturing Engineering QA Lead (Winnipeg)
🏢 Sonova Group
📍 Winnipeg