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.

Requirements

Requirements • A Spirit of Cooperation and team working. • Ability to plan and manage own work. • Experience In Pharmaceutical Field Would Be An Advantage. • Time management and high attention to detail and accuracy. • Pro-activity and hard-work. • A Spirit of Responsibility. • Field Of Study: Chemistry- different field of engineering and any related field. • Proficient in Windows & Office Tools. • Good command in English specifically in verbal communication and technical writing skills • Familiarity with many aspects of validation is expected. • Educational Level: BSc or MSc

Employment Type

  • Full Time

Details

Employment type

  • Full Time

Educations

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