Pharmaceuticals Consultant -QA

 Pharmaceuticals Consultant -

https://sites.google.com/view/pharmava/home

1. Performing in-process quality assurance (IPQA) checks for tablets, capsules and liquid orals.

 2. Participation and issuing of line clearance at every step of batch manufacturing. 

3. Preparation, Maintaining and updating the Batch Manufacturing Records(BMR)/BPR Documentation of log books, calibration records, temperature and humidity records etc.

4.  Assisted in production of various products. Preparation, Review, distribution and retrieval of Standard Operating Procedure (SOP) and its Formats. 

5. To carry out routine inspection of all departments for GMP Compliances. Handling of Corrective and Preventive Actions (CAPA). 

6. Controlling all the documents related to QA. 

7. Handling of Change control. Preparation and review of Annual Product Reports. 

8. Preparation of Master Formula Record (MFR)/ Master Processing Control Record.

9.  Issuance and Review of Batch Manufacturing Record (BMR) and Equipment Log. 

10. Review of daily checklist like weighing balance, cleaning entries, environment monitoring, etc. 

11. Preparation of Validation Master Plan (VMP); Sampling and Report preparation for Process Validation. 

12. Review of Analytical test report, raw data and issuance all format related to QC. 

13. Handling of deviation. Checking and Release of Finish Product for dispatch. 

14. Documentation and checking of artwork. 

15. Preparation and documentation for grant of permission to manufacture a new drug (FORM 44) to DCGI. 

16. Preparation and documentation for license to manufacture drugs for purpose of examination, test or analysis (FORM 30) to SLA. 

17. Preparation and documentation for ENDORSEMENT OF ADDITIONAL DRUG to SLA.

QA professional is to assure that medicinal products are designed and developed in a way that meets the requirements of Good Manufacturing Practice (cGMP).