Neslihan Sarialtin

To prepare CE technical file & design file/To ensure the continuity and development of ISO 9001 QMS/To organize controlling activities according to ISO 13485 and MDD requirements/To follow the international regulations of the products, legislations published by the Ministry of Health/Follow up to date the standards published by the auditor bodies and the Competent Authorities/To inform the departments if necessary/To take part in internal audits as auditor/To manage meetings in terms of QMS and R&D

To perform the documentation& application according to ISO 9001 Quality Management System/ To regularly follow the related tests and necessary quality control documents in the atelier (small firm) which produce liquid hand soap/ To perform the duties assigned by the Quality Control Chief/ Checking and reporting product quality/To keep records of all control procedures and tests/Taking, labeling and archiving the required samples/To submit new proposals for quality improvement activities