JOB OBJECTIVE

Responsible of ensuring to control, monitor and record all activities which directly or indirectly impact on all aspects of the product quality, donor suitability and donor safety, as well as plasma testing and plasma warehouse.
Responsible of implementing suitable controls to ensure the accuracy, integrity, availability and legibility of documents.

KEY RESPONSIBILITIES

• Prepare and review SOPs 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 ...