Duties&Responsibilities:

 

Preparation of site master file Generate standard operating procedures. Receipt, and handling of any compliant (Market/ Supplier) Prepare APR Perform internal audits for all technical departments External audits for local packaging materials suppliers. Follow up site CAPAs implementation and closure Receive, discuss, evaluate, and set action plans for raised change controls Follow up change control action plans implementation and closure Follow-up training system implementation & proper documentation following the current approved training procedure in all technical departments Conducting GMP, GDP, Data integrity trainings Handling recalls

 

Qualifications:

 

Bachelor’s degree in Pharmacy / natural Science or any related field. 3 – 5  years of experience in a quality role or related field.