
Auditor/Technical Expert(MDR)
- İstanbul
- Sürekli
- Tam zamanlı
- Conducting quality system audits for medical device manufacturers
- Assessment of MDR compliance and review of technical documents
- Providing technical support for decision-making processes related to certification
- Preparation of MDR technical documentation and operation of the quality management system in accordance with the requirements of the Medical Device Regulation MDR 2017/745
- Monitoring regulations regarding medical devices and implementing relevant arrangements.
- Bachelor's/Master's degree in biomedical, biotechnology, engineering, or other science fields
- Minimum 4 years of work experience in the medical device industry, including at least 2 years related to quality management
- Experienced in Design Development, Production Process Control, Document Management, Risk Management, Corrective/Preventive Action Management, and Change Control Management systems
- Knowledge of post-marketing surveillance systems (PMS, PMCF, PSUR, etc.)
- Experienced in ISO 9001, 13485, ISO 14971 CE, and MDR regulations, and actively involved in Quality Management System activities.
- Strong analytical thinking and technical reporting skills
- Excellent written and spoken English skills.