Responsibilities & Duties:
•    To perform Audits to all critical suppliers according to the established program. 
•    To carry out GMP audits of critical suppliers, subcontracted activities as well as corporate audits of Blood establishments and GMP systems.
•    To receive 3rd party audits as well as Health Competent authorities’ inspection.
•    To evaluate critical suppliers according to the established procedures based on Audits performance result and KPI’s (Key Process Indicators)  established for measuring level of cGMP compliance of product as well as services received.
•  To ensure that Documents containing instructions should be approved, signed and dated by appropriate and authorized persons. 
 

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.