Job Overview
-
Date PostedApril 9, 2023
-
Location (State / UT)
-
Expiration dateAugust 5, 2024
-
Experience2 Years, 4 Years
-
GenderAny
-
Desired QualificationBachelor Degree, Master’s Degree
Job Description
Executive Quality Control
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.
The following will be the responsibilities of the position holder:
- Analysis of Stability Samples/ Finished Products as per respective STP/Specification in Quality Control of Hormone block.
- Calibration of routine usage instruments such as Balance, pH meter, and Conductivity meter, as and when required.
- Timely analysis of stability sample (Hormone block) and report if any abnormality is observed.
- Timely Charging & withdrawal of samples from Stability Chambers & their documentation within the time frame.
- Sample reconciliation and destruction record of stability sample.
- Implementation of GLP / GMP requirements.
- Coordinating and aligning the practices and procedures in line with the COBC requirements
- Stability sample charging, Withdrawal, Reconciliation, and data entry in software such as LIMS.
- Completion of assigned training of GLP/GMP on time
- Reporting of stability/Finished product sample as per report received from outside Laboratory and checking the compliance against respective specifications.
- Evaluates the analysis results as per SOP and report to the supervisor for any abnormality.