Job Description

1. Monitoring of the sampling activities in the validation batches. Essential oils and carrier Oil 2. Receiving Raw materials / packing materials and keeping that material on proper place and their entries in Log books. 3. Receiving packed material from packaging department and keeping that material on proper place, and their entries in Log book. 4. Responsible for Document Archival & up keeping. 5. Preparation of Certificate of Analysis for Dispatch as per Sale order. 6. To work & implement the cGMP practices in to all departments as per SOPs. 7. Preparation of SOPs & relative documents. 8. To check the status of dispatching material and maintain its log-book. 9. To maintain record of all log sheets of production area. 10. To maintain the record of raw material finished goods, Inward sample. 11. To check the status of each equipment. 12. Other QA related activities. Should have testing knowledge of: A) Refractive index B) Optical Rotation C) Specific gravity, weight/ml D) Acid value, peroxide value, saponification and un saponification, water content, melting point and boiling point etc. E) Gas Chromatography, 13. Follow any other duties which will be assigned by the management time to time. Job Type: Full-time Salary: From 925,000.00 per month Benefits:

• Leave encashment

Schedule:

• Morning shift

Application Question(s):

• Are you from chemistry or Pharma background
• Do you have knowledge of Titration or documentation like Fill BMR, Questionnaire etc

Education:

• Bachelor\'s (Preferred)

Experience:

• total work: 1 year (Preferred)