Klaston Management is seeking a highly qualified professional to perform internal audits in accordance with ISO 13485 (Quality Management Systems for Medical Devices).

Main Responsibilities:

- Plan, conduct, and document internal audits in compliance with ISO 13485 requirements;
- Assess the effectiveness and conformity of Quality Management Systems;
- Identify nonconformities, risks, and opportunities for improvement;
- Prepare explicit, accurate, and complete audit reports;
- Monitor and support corrective and preventive action processes;
- Maintain professional and ethical communication with clients and internal stakeholders.

Knowledge, Skills, and Abilities:

- Highly organized professional with strong attention to detail;
- Ability to work independently and manage multiple priorities;
- Availability for domestic and international travel;
- Valid passport and driver’s license;
- Minimum of three (3) years of proven experience conducting ISO 13485 audits;
- ISO 13485 Lead Auditor Training Course (mandatory);

If you're interested please send your CV to [email protected]

📌 ISO 13485 Lead Auditor (Ontario)
🏢 Klaston Management
📍 Ontario