Responsibilities & Duties:
•    Prepare and review SOP’s related to Documentation Lifecycle Systems following the guidelines established according to Egyptian regulations and the guidelines established according to cGMP requirements and Good Documentation Practices
•    Compile all the information related to  Documentation Lifecycle referred to Key Process indicators established for the Quality system.
•    To define a system of control of documentation that ensures that documents within the Quality Management System should be regularly reviewed and kept up-to-date.
•    To ensure that documentation should be designed, prepared, reviewed and distributed with care. The reproduction of working documents from master documents should not allow any error to be introduced through the reproduction process.
•    To ensure that Documents containing instructions should be approved, signed and dated by appropriate and authorized persons. Documents should have unambiguous contents and be uniquely identifiable. The effective date should be defined.
 

Requirements:
•    Bachelor ‘s Degree in Health-related Sciences
•    Knowledge of Quality Management, as Good Documentation Practices
•    Knowledge of cGMP requirements preferred
•    Typically requires a minimum of 2 years of related experience  in GMP Documentation Systems within a Pharmaceutical Company preferred. 
•    Proficiency with computers
•    Written and spoken English and Arabic.