Quality Documentation Specialist

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 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. KEY RESPONSIBILITIES - Bachelor s Degree in Health-related Sciences. - Knowledge of Quality Management, as Good Do