Job Description

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.

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