ÖZLEM SAVRAN

• Completed training Basic Management and Organization, Digital Transformation, Advertising and Marketing and Project Management.
• I prepared a portfolio that includes the following documents: Organization File, Project Initiation Document, Critical Path Method, Risk Management Plan, and Project Timeline.

Tools Used

• Excel
• Miro
• Word

• Cross-trained in multiple departments, including Quality Control and Sales, performing various tasks following established procedures
• Acquired strong expertise in Turkish medical device regulations and ISO standards compliance
• Contributed to the production of Class I medical devices, including both sterile and non-sterile products, ensuring adherence to relevant regulations and quality standards
• Formulated and documented weekly work plans using MS Excel for efficient task management
• Implemented control procedures and verified compliance with production work order specifications
• Acquired basic experience in using NETSİS for accounting and financial management tasks
• Managed data entry and tracking of medical devices using the Turkish Product Tracking System for accurate product registration and traceability
• Collaborated with international companies via email to facilitate project discussions and enhance business relationships

• Assisted in the development and testing of biomaterials for medical applications, focusing on bone regeneration
• Gained hands-on experience in laboratory procedures, including material characterization and quality testing
• Acquired knowledge of regulatory requirements for biomaterials in medical device applications