2 - 7 years
4.0 - 9.0 Lacs P.A.
Tarapur, Ankleshwar, Hyderabad
Posted:2 months ago| Platform:
Work from Office
Full Time
In-Process Quality Assurance During Production Activity Including Line Clearance And Sampling At Different Stages Of Processing/Packing As Per Pharma API Review of Master Documents such As BMR / BPR Test Batch Monitoring Process Validation Protocol Required Candidate profile Experience with reputed API or Bulk Drugs Unit Co-Ordinate with Plant QA And RA for PDR related activities To Review Specification, MOA And Analytical Data Good Computer And Communication skill Etc
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