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Quality Manager in Medical Device Manufacturing
Job Description & How to Apply Below
This role is essential for overseeing quality programs, guiding Quality Engineers, Inspectors, and Technicians, and ensuring adherence to FDA requirements. You will lead cross-functional investigations of complex quality issues while partnering with Operations to identify compliance risks and implement solutions that foster manufacturing excellence.
Key Responsibilities:
• Lead Quality team performance and development initiatives
• Ensure compliance with FDA (21
CFR
820) and ISO standards
• Oversee production quality programs and process controls
• Drive continuous improvement through data and metrics reviews
• Manage design transfer activities from NPD to production
Requirements:
• Bachelor’s degree with 8+ years of Quality experience
• 4+ years in production quality roles
• 3+ years in the medical device industry
• Proven experience as a people leader
• Ability to lift up to 35 pounds
Enhance production quality and compliance in medical device manufacturing with Verathon's dedicated team in Burnaby.
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