5 - 10 years
4 - 9 Lacs
Posted:8 hours ago|
Platform:
Work from Office
Full Time
1. Stability study documents compilation and its management.
2. Stability charging, withdrawal, trend and stability report preparation.
3. Review of DRS, Log book entry and related documentation to be make online.
4. Preparation of release COA and compilation of all related documents.
5. Provide training to new person or existing person for QC testing.
6. Preparation and review of Specification/STP/SOP/DRS/protocol/data recording sheet for QC documentation on routine basis.
7. Instrument and Equipment calibration activity.
8. QMS (change control/deviation/Incident/LIR etc.) related Activities.
-Male Candidate Required
-Candidate should have experience in Biotech or injectable industry.
Intas
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