Job Description
Should have Knowledge on Wet instruments & HPLC, GC, Dissolution, DT, Friability, FTIR, UV-Vis. Spectrophotometer, Hardness tester, Auto titrator, desirable validations for assay, related substances, .
Required Candidate profile
Candidate have an Exp in API or Intermediates or Bulk Drug Industries in QC Dept - 1 to 8 yrs Exp - Chemist to Sr.Executive up to reviewer position exp faced USFDA, other regularity audits and Wet analysis, HPLC, GC Exp and document reviewing in API
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