Job Description
1. To approve or reject, as sees fit, starting materials, packing materials, intermediate, bulk and
finished product.
2. Checking & approval of finished product reports.
3. Preparation & approval of standard operating procedures in quality control.
4. Preparation & approval of specifications & method of analysis for raw materials, bulk & finish
products.
5. Documentation of finished products.
6. Documentation & maintenance of samples for stability study.
7. Overall documentation of quality control
8. Communication to public testing lab.
9. Stability sample sending to public lab
10. Preparation of analytical chemist validation and maintaining the records for the same.
11. To ensure that all necessary testing is carried out and the associated records evaluated.
12. To approve specifications ,sampling instruction ,test methods and other Quality Control
Procedures
13. To approve and monitor any contract analysts.
14. To ensure the qualification and maintenance of the department, premises and equipment.
15. Preparation of excel sheet validation.
16. Checking of all instrument calibration records and prepared the calibration schedule.
17. To ensure that the appropriate validations are done.
18. To ensure that all necessary testing is carried out and the associated records evaluated.
19. To approve specifications ,sampling instruction ,test methods and other Quality Control
Procedures
20. To ensure that the required initial and continuing training of his department personnel is carried
out and adapted according to need.
21. Checking of all instrument calibration records and preparation of calibration schedule.
22. Daily job allocation
Employement Category:
Employement Type: Full time
Industry: Pharmaceutical
Functional Area: Quality Control
Role Category: Other - Quality Assurance
Role/Responsibilies: Quality Control
Contact Details:
Company: Cheryl Laboratories
Location(s): Mumbai
Keyskills:
Quality Control
Documentation
Qc