Posted:2 days ago|
Platform:
On-site
Sr. No.
Job Responsibilities
1
Have a knowledge on Quality control function like FP/RM/PM/Stability of Solid dosage forms.
2
Having a good knowledge on QC Instrumentations
3
Having sound knowledge on trouble shooting of QC instruments like Auto titrator, HPLC, GC etc.
4
Expected knowledge of 21CFR part 11 compliance and Computer system validation
5
Must having knowledge on Investigation like OOS, OOT, events and deviation management.
6
Having knowledge on LEAN management and Good presentation skill
7
Having exposure on Regulatory Audit handling and management
8
Regular review of SOPs versus practices for gap analysis.
9
Trending of QC data and deriving action plan for compliance readiness
10
Having good exposure of review of analytical raw data
Sun Pharma Laboratories Ltd
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