Lab Assistant
Glaxo Saudi Arabia Ltd
Total years of experience :7 years, 5 Months
1. Receive Samples from Production & QA-Compliance & place them in the sample cabinets after the necessary login in the sample receive logbook.
2. Preparing & applying labels of products and raw materials for QC planning board.
3. Printing RMA/BAR (Lab testing template) from Document Management System and compiling the lab documents along with Receiver Tickets and CofA, then prepare them for Chemist/Sr. Chemist for testing.
4. Preparing & applying status labels after approval of QC Section Head to Raw materials in the warehouse.
5. Maintaining Receiver ticket archive cabinets to file these documents.
6. Submit the completed Lab documents to QA-Compliance for final batch release.
7. Entering Critical QC test parameters of APIs & ‘A’ Products into the ‘Trend’ folder before submission to QC Section Head for Approval.
8. Enter ‘Raw, RO & Purified Water’ results to designated folders for QC Review.
9. Organizing the guidance’s and references files.
10. Receive retained sample of raw material from QA-Compliance and register into the Retained Sample Logbook.
11. Support Compliance Department in collection raw material and C&D Products samples. When required.
13. Support QC Section Head and all QC Staff as & when required.
14. Coordinate with HR and Procurement for QC Lab when needed.
15. Maintain the hazards assessment file.
16. Maintain the supplier’s files to have records of quotation and any correspondences with them.
17. Update QC Lab activities files every year & archive old one in the QA Compliance department till their retention period.
18. Support in destructing the raw materials & finished products samples after testing.
19. Update the QC KPI Board.