Quality Documentation Specialist

Grifols Egypt for Plasma Derivatives

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 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 in Computers.

- Organized and able to manage time effectively.

- Ability to work within a highly regulated, labor-intensive environment.

- Ability to understand, explain, follow, and enforce SOPs and protocols

- Ability to plan, communicate and execute activities for the improvement of overall operations.

- Written and spoken English and Arabic.