Sr. Operating Supervisor

Tabuk Pharmaceuticals Manufacturing Co

1. To follow up the instruction from production Officer/supervisor/senior supervisor.

2. To check the availability of packing POIs and the related packing material for starting the concerned batch/product.

3. To follow up and arrange the QA notification along with the green release label.

4. To arrange the related manufacturing POI.

5. To calculate and segregate the tablets/capsules as per the requirement of POI for different consignees.

6. To follow up the documentation of the concerned area logbooks, POI and WIP logbooks.

7. To follow up the return of packaging materials after completion of the batch.

8. Inform production Officer / production supervisor / senior production supervisor for occurrence of any breakdown.

9. To raise the Job Order in case of any maintenance or breakdown.

10. To ensure the correct tablets/capsule drums, correct foil/PVC and correct quantity are being brought before starting the batch.

11. To raise the requisition slip for any additional requirement of packaging materials.

12. To work on machine as an operator if concerned operator absent or due to the shortage of the operator.

13. To relieve the machine operator during break if any.

14. To help the machine operator during machine setting or if any problem persists.

15. To check the cleanliness and documentation of machine as per related SOP-PRD-068 & SOP-PRD-032.

16. Monitoring of GMP practices of subordinates such cleaning, hygiene and gowning

17. Ensure that in process control being conducted according to POI and SOP frequencies

18. Raising deviation in case of non-conformity observed.

19. Conduct investigation, quality risk assessment & CAPA proposal

20. Report to production management all nonconformities observed in the area or processes

21. Raise change control and conduct impact assessment for production part prior final approval by QA

22. Conduct GMP & SOP training for subordinate

23. Ensure line clearance & stage approval being conducted as per SOP requirements and standards

24. Ensue documentation correctness in batch records, logbooks and GMP records to maintain data integrity in the area

25. Ensure environmental conditions in the area