7 - 9 years
4 - 6 Lacs
Posted:7 hours ago|
Platform:
Work from Office
Full Time
1.Issurance of BMR,ECR to production Department.
2. Issuance ofprotocol to QC deparlment & other formats to respective department. 3.
Issuance offinished product labels and seal.
4. To maintain, check and retention fi1led BMR, QC reports, formats and other filled records that are
received from production, quality control and other departrnents.
5.To issue and Handling of change control,deviation,OOS reports and maintain their records.
6.To co-ordinate durins intemal audit.
7. To take QA round or as per SOP's.
8. To do any other supporting work in absence of any other staff from department as per instructior
given by department head.
9. To prepare and review master documents such as BMR, MFR, SOP's and other documents.
10. To prepare and review validation protocol and report.
11. To prepare and review annual product quality review (APQR).
12. To prepare and review RA related documents.
13. Comnliance for audit observation.
14. Risk analysis protocol & report preparation.
15. In absence QA manager Release and dispatch co-ordination along with QA/warehouse and
SANVIN group
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