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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
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.
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