Skills: Mastery and identification of products Proficient in the regulations of the Food and Drug Organization Effective communication skills Being responsible and full of energy Mastery of pharmacopoeias and pharmaceutical standards Mastery of documentation and report writing Familiarity with TTAC
Job description and duties:
Mastery of GMP requirements Complete mastery of compilation, control and archiving of quality assurance documents Mastery of quality management system processes Familiarity with BPR documentation Creation and modification of manufacturing licenses for all products by applying the changes received from the relevant units and following up and completing the documents related to the Food and Drug Administration and paying the license issuance costs in order to update and complete the process. Obtaining or renewing product licenses Documenting and filing all related reports and SOPs issued by the quality assurance unit Receiving and following up on matters related to samples based on the samples sent from the supply unit Preparation and compilation of necessary reports through data and information review.