Job Description


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

Employment Type

  • Full Time

Details

Employment type

  • Full Time

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