QA compliance specialist
Future pharmaceutical industries
Total des années d'expérience :7 years, 7 Mois
• Check the dispensing process and ensure that all materials are dispensed according to batch record
• Monitoring temperature, relative humidity and differential pressure of production area, warehouse area
• Check up of clearance and cleanliness of all production rooms and sampling room in warehouse area
• Check and follow the production to ensure their behavior and hygiene according to GMP rules.
• Responsible for activities such as: sampling and documentations.
• Labeling all raw materials, packaging materials and finished product in warehouse area
• Labeling all intermediate products in production area.
• Check up the moisture content of the powder of intermediate products.
• Follow up the weight, hardness, friability, disintegration tests during the production of tablet dosage form.
• Follow up the leakage test during blistering process.
• Follow up the weight test of capsule and powder dosage forms.
• Sampling the intermediate products during the production process.
• Samples all starting, packaging and finished products to be retained in the retained samples room.
• Batch record review
Follow up production lines to make sure of the products' quality
Department : Microbiology & Chemistry Overall grade : very good