Chemical Expert

Job Description

• Analyzing new products, control, and approval of the relevant documents.
• Preparing, and controlling validation documents for analytical methods.
• Preparing manufacturing methods for new formulations, determining critical points and control strategies.
• Following up on approval of product scale-up reports.
• Implementing  stability studies of new formulations, control, and approval of relevant reports.
• Implementing  in-vitro studies of new formulations, control, and approval of relevant reports.
• Implementing  product formulation modification process with the quality risk management approach.
• Following up on approval of all required documents of the research and development laboratory needed to be sent to the Food and Drug Organization.
• Determining the specification of starting materials and packaging materials required for new formulations.
• Working in a friendly environment in the laboratory promotes a spirit of cooperation.
• Implementing elements of quality management systems such as deviation management and change management based on defined internal procedures.