Job Description
-Supervising the preparation of BATCH-HISTORY according to the set criteria and liberalizing the distribution
-Carrying out all the procedures for obtaining the manufacturing license of new drugs and taking timely action to renew the manufacturing license of current products according to GMP regulations.
-Receiving reports of periodic inspections of the MOH in order to correct and eliminate deficiencies and follow up to eliminate deficiencies and report corrective actions
-Receiving and communicating all the criteria of the Ministry of Health, Treatment and Medical
-Monitor and control all necessary manufacturing, packaging and associated documents, test and release of the produced batch of products.
-Planning for continuous modification and improvement and carrying out internal inspection
-Supervising the implementation of the rules for ordering raw and packaging materials
-Submissions to the MOH, product registration, consumer information and all regulatory activities
