QA Executive / QA Manager

Experience: Minimum 4-6 years

Education: Graduation; Post Graduation: BSC/B.Pharma/M.Sc/M.Pharma

Desired Candidate Profile:

Required experience of 4-6 years, Exposure to work with one or more reputed organization. Knowledge of line clearance, process check during manufacturing and packing, Documentation, review of BMR and BPR.

Job Description:

Designation: QA Executive/Asst QA Manager (DOCUMENTATION/IPQA)

Work Profile:

1. Res To Perform Line clearance & Inprocess Quality assurance related activities during Tablet, Capsule & Transdermal manufacturing

2. To Perform Line clearance Inprocess Quality assurance related activities during Tablet, Capsule & Transdermal packing.

3. To ensure that Good Documentation practice is followed at shop floor (Ground floor) during data recording in logbooks, Bach Records etc.

4. Responsible for Internal audit of Ground floor production area.

5. Responsible for Maintenance of Quality assurance Records related to Ground floor Production area.

6. To perform calibration of IPQA instrument at ground floor in timely manner & report to seniors about any discrepancy.

7. Responsible for Dispensing of Raw Material & Packing Material.

8. To ensure that production activity is carried out with properly calibrated/validated/Qualified equipment.

9. To ensure preventive maintenance of Ground floor equipment is carried out properly in timely manner

10. To report any deviation & discrepancy in area & activity.

11. To supervise on line documentation for Tab./Capsule/Injection / Transdermal patches etc.

12. Review of BMR & BPR s of Tab. / Capsule / Injection / Transdermal patches up to FG Transfer and preparation of Dispatch Note.

13. Responsible for Retrieval of Batch Records & logbooks in timely manner.

14. To ensure the compliance of systems during manufacturing, packing and testing of products as per quality standards.

15. Responsible for supervision & sampling during Process Validation batches & any other validation activity.

16. To ensure proper sampling during Validation activity/Routing manufacturing etc.

17. To ensure compliance of SOP s at Ground floor production area.

18. To attend GMP, SOP & general & Job specific trainings.