Quality Auditor
1 day ago
An experienced ISO 13485 Quality Auditor with substantial experience in QMS and factory auditing is required to do technical, QMS, and compliance audits on medical devices. You should be highly proficient in conducting deep reviews of production processes and be able to communicate well with all organisational levels – from production staff to executive management.
Responsibilities:
- Perform on-site ISO 13485 QMS audits of the production facility
- Review quality management protocols
- Evaluate production processes for compliance with quality requirements
- Complete audit reports, including documentation of non-conformances and improvement opportunities
Requirements:
- Quality audit experience
- Experience in manufacturing environments
- Deep knowledge of medical devices production, ISO 13485, GMP standards, and quality management practices
- Experience working and communicating with senior management levels
About AMREP:
AMREP Supplier Management Services is a global third party supplier quality management company with a proud history of achieving our clients' production and quality objectives.
Seniority levelMid-Senior level
Employment typeFull-time
Job functionQuality Assurance
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