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Job Description

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.

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