Carrying out matters related to obtaining a license to manufacture new drugs and renewing current drugs Submitting inspection reports and taking action to eliminate deficiencies and conduct periodic internal inspections Supervision and control of documents of each batch of manufactured products (and contract production) Formulation and compilation of production documents and preparation of SOP and efficiency of HVAC system and water consumption in production Comply with GMP principles Development of methods for controlling and manufacturing raw materials, packaging and storage of semi-finished goods and final products Releasing raw materials and packaging for consumption Release of the final product Observance of implementation of GMP.GSP.DMF standards in the fields of: matching physical specifications and packing incoming items to the warehouse Moving materials from the warehouse to the units and leaving the factory General conditions such as cleaning and special conditions such as arrangement of warehouses and weighing section
Requirements
• Ladies / gentlemen: 1 person
Minimum age: 30 years
Familiar with FDA protocols
• Has a general doctorate degree in pharmacy and is not prohibited from presenting a technical manager's license
• Has the necessary knowledge about GSP, GMP, GLP, CTD and SOP coded methods and monitoring the performance of HAVC system and batch record and analysis
• Lack of simultaneous employment in other pharmaceutical institutions and companies simultaneously
• At least three years of relevant work experience