2 - 7 years
3 - 6 Lacs
Posted:6 hours ago|
Platform:
Work from Office
Full Time
To check and certify line clearance.
To ensure Cleanliness for the GMP areas.
To perform in-process sampling and testing.
To ensure timely record of the data and proper arrangements of documents.
Review of Batch Manufacturing Records/ECR/Analytical Documents.
Sampling of Finished Product and its respective records. Ensure that compliance with existing SOPs, cGMP/cGLP.Perform other work allocated by designated person.
A Person should be having knowledge about the current guideline.
Good Communication Skills.
Knowledge of GMP is a must.
Dishman Carbogen Amcis
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