Job Description
• Understanding the Basic Principles of GMP and Internal Auditing.
• Knowledge of the activities carried out in the pharmaceutical industry.
• Good Documentation Skills
• Responsible for preparing and executing validation documents and Protocols. Protocol development skills will include ability to develop Installation, Operational and Performance qualification documents.
• Performing validation (or Qualification) and calibration for equipment such as Autoclave, HPLC, UV-vis, temperature and pressure gauge.
• Understanding the Needs of the Quality Assurance Unit
• Identification of the Data Analysis of the Various Units.