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Job Location | Indore |
Education | Not Mentioned |
Salary | Rs 2.0 - 4.0 Lakh/Yr |
Industry | Pharma / Biotech |
Functional Area | Quality (QA-QC) |
EmploymentType | Full-time |
EXECUTIVE - QC1. Review of RM, PM &FP Specifications, and STPs & Data sheets.2. COA checking & final report approval.3. Co-ordination with public approved laboratories4. Approval in register / software after final review of FP reports.5. Updating of SOPs.6. Preparation of new SOP7. Training to subordinates.8. Final approval of RM , PM & FP reports9. Review of documents and protocols10. Work allocation in FP section11. Handling of Lab incidence in FP section12. Daily verification, GLP and calibration of all QC Instrument as per calibration Schedule.13. Review and checking of all daily and monthly calibration records.14. Receipt of column, impurities, Reference standard and proper upkeepment of the same.15. Preparation and archiving document related to working standard.16. Preparation and revision of SOP, STP and Specification.17. Planning, preparation and coordination of training in QC Department.18. Receipt of chemicals and maintain the records.19. Checking and review finish product report, STP and Specification.20. Maintain the document related to all instrument in QC.21. Follow up with parties for breakdown of instruments.22. Checking SOP compliance in QC Dept.Desired Candidate Profile :2-5 years of work experience.Educational Qualification : B.sc/M.sc (Microbiology )Perform QC analysis/other routine microbiological testsLocation: Bhopal (Mandideep)
Keyskills :
documentationquality controlpharmastphplcmicrobiologycalibration