ISO 13485 Auditor and Consultant
1 week ago
The ideal candidate for this role will have a proven track record of ensuring high-quality standards in medical device production. As an ISO 13485 Quality Auditor, you will be responsible for conducting audits of production facilities, reviewing quality management protocols, and evaluating production processes for compliance with quality standards.
Key Responsibilities:
- Conduct thorough on-site audits of production facilities
- Review and analyze quality management protocols
- Identify areas for improvement and develop corrective actions
- Collaborate with cross-functional teams to implement quality improvements
Requirements:
- Minimum 5 years of quality audit experience
- Expertise in ISO 13485 and quality management principles
- Excellent analytical and problem-solving skills
- Ability to communicate complex information effectively
About AMREP Supplier Management Services:
As a global third-party supplier quality management company, we are committed to helping our clients achieve their production and quality objectives. Our team of experts works collaboratively to provide tailored solutions that meet the unique needs of each client.
Seniority levelMid-Senior level
Employment typeFull-time
Job functionQuality Assurance
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