About the Role
Experience Required: B.Pharm / M. Sc. with 2-4 years of experience in Chemical & Instrumental analysis QC (Finished goods & stability). Approved chemist licensed candidate shall be preferred. Well versed with CAPA, GMP Documentation, should have exposure to regulatory audits such as MHRA, USFDA etc.
Followings will be the responsibilities of the position holder:
1. Analysis of Stability Samples/ Finished Products as per respective STP/Specification in Quality Control of Hormone block.
2. Calibration of routine usage instruments such as Balance, pH meter and Conductivity meter, as and when required.
3. Timely analysis of stability sample (Hormone block) and report if any abnormality observed.
4. Timely Charging & withdrawal of samples from Stability Chambers & their documentation within the time frame.
5. Sample reconciliation and destruction record of stability sample.
6. Implementation of GLP / GMP requirements.
7. Coordinating and aligning ...
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