工作内容 ：
1.按照客户的审核标准到现场进行质量控制和审核，撰写相关的审核报告并上传至公司。
2.组织或参与审核，实施审核工作。
3.评估客户的符合性，以便发放或维持认证
4.在审核结束后，或在指定的时间范围内，确保及时完成好的质量报告（包括费用申报）。
5.确保认证的后续工作。
6.促进知识共享。
1. Conduct quality control and audit to production site according to customer's audit criteria, write related audit reports and upload them to the company.
2. Organize or participate in the organization of the audit; Carry out the audit.
3. Assess client compliance in order to issue or maintain certification
4. Ensure timely production of good quality reports (including expenses claims) directly after the audit close-out, or within the designated time-frame (for referential demanding
5. Ensure the follow-up of the certification
6. Contribute to the sharing of knowledge

工作要求 ：
1.本科及以上学历，生物、医学类相关专业。
2.至少持有QMS质量管理体系外审员资格证书。
3.具有5年以上医疗质量管理或研发类工作经验。
4.具有13485医疗器械管理体系相关证书。
5.良好的英语交流及报告书写能力。
6.驻华南地区为佳，能够接受出差。
7. 为人正直，品貌端正；具备良好的沟通和学习能力。
1. University graduate majoring in Biology/medical /science/physician.
2. At least ISO9001 QMS external auditor.
3. At least 5 years working in medical quality assurance / R&D.
4. ISO 13485 certificate, and MDQMS audit related experience is preferred.
5. English is ok to communicate and report;
6. Locate in South/ Guangdong is preferred, accept business travel.
7. Honest, have good appearance, communication and learning ability.

其他信息


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