Job Overview
-
Date PostedOctober 22, 2023
-
Location (State / UT)
-
Expiration dateJanuary 17, 2025
-
Experience6 Years, 9 Years
-
GenderAny
-
Desired QualificationBachelor Degree, Master’s Degree
Job Description
Role & responsibilities:
- The candidate should be an expert in reviewing analytical, validation, and qualification reports of quality control.
- Experience working in LIMS, QMS, and Chromelon 7.2 software.
- Exposure to work in regulatory environments such as USFDA, MHRA, TGA, ICH, and PICS.
- Experience Planning, allocation, and investigation of stability sample analysis.
- Exposure of handling the charging and withdrawal of stability sample into the stability chamber.
Desired Candidate Profile:
- B.Pharma, B.Sc, M.Pharma
- 6-9 Years of Relevant Experience.
- Salary: 5.50-8.50 L CTC/PA