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PHARMA JOBS POST > Vadodara > Exemed Pharmaceuticals hiring for Sr.Executive in QC department @Vadodara
Vadodara

Exemed Pharmaceuticals hiring for Sr.Executive in QC department @Vadodara

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Last updated: April 21, 2022 1:37 am
ADMIN 3 years ago 50 Views
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Exemed Pharmaceuticals hiring for Sr.Executive in QC department @Vadodara

Company Name – Exemed Pharmaceuticals
Location – Luna ,Dabhasa (Vadodara)
Designation – Sr Executive QC
Experience – 7 to 12 years (PHARMA API CO)
CTC- Open
Company Profile :  www.exemedpharma.com
Job Description – Mentioned below 

If interested pls mail CV on [email protected]

1. Compliance of USFDA.

2. To develop, and verify specifications, standards, sampling instructions, test procedures for physical, chemical, and any other testing, or any other laboratory control mechanisms.

3. Review of raw analytical data and analytical protocols.

4. Sampling & analysis of Raw materials, Packing materials, Intermediates, final products and update its status.

5. Analysis of R&D samples, DM Water and effluent water.

6. Analysis of stability / Hold time study samples and market samples.

7. Ensure that all necessary testing carried out as per specifications.

8. Preparation of reagents and standardization of volumetric solutions and maintenance of its records.

9. Qualification of working standards and maintenance of its record.

10. Instrumental testing, calibration and validation.

11. Line clearance for production activities in Shift.

12. Analysis and Release of in-process samples during shift.

13. Reporting of deviation, out of specification results as and when observed, its investigation and CAPA.

14. Updating of specifications and SOPs.

15. Participate in validation and qualification activities.

16. Preparation of yearly instrument calibration schedule.

17. Calibration and maintenance of analytical instruments as per schedule

18. Review and update existing SOPs as per cGMP wherever necessary.

19. Training and development of quality control personnel.

20. Checking and verification of all analytical reports of raw materials, packing materials, in-process and finished products. Checking the stability / Hold time study protocols and report of finished products.

21. To see that all the necessary equipment required for testing are in proper state.

22. Vendor auditing.

23. Conduct and record periodic internal audit in order to monitor the implementation of quality and environmental management system and propose any necessary corrective measures.

24. To maintain the discipline in the department

If interested pls mail CV on [email protected]

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