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 complianceSupport collaboration for design and validation tasksPrepare for audits and manage CAPA processesTrend analysis of quality metrics for improvementsCoordinate quality resolutions for nonconforming productsRequirements:Master's degree in engineering or quality fieldMinimum 4 years of quality experience in medical devicesProficiency in ISO standards and regulatory guidelinesStrong problem-solving and stakeholder management skillsProficient in MS Office and eQMS platformsDrive quality assurance excellence at Sonova and make a significant impact on operational metrics.

📌 Sonova Manufacturing Engineering Qa Lead (Kitchener)
🏢 Sonova Group
📍 Kitchener