Join Intertek as a Lead Auditor specializing in Medical Devices with extensive travel required. You will focus on compliance audits and support development across client systems.

This full time home-based role requires a minimum of 6-10 years in the medical device industry. As a Lead Auditor, you will assess client management systems against ISO 13485 and other international standards. Expect to engage with clients, provide technical training, and lead audit teams while ensuring adherence to regulatory requirements.

Key Responsibilities:
• Audit compliance with ISO 13485 and regulations
• Provide technical support and training for Auditors
• Liaise with clients on audit activities
• Review quality management system documentation
• Present audit results to clients and certification boards

Requirements:
• 6-10 years in the medical device industry
• 4+ years in quality management systems
• Excellent communication and analytical skills
• Willingness to travel extensively
• Bachelor's degree in relevant field

Bring your expertise in quality assurance and compliance to contribute to Intertek's mission of excellence.
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📌 Lead Auditor for Medical Devices (Quebec City)
🏢 Alltech Consulting Services
📍 Quebec City