The QC Incharge is responsible for the timely and accurate chemical and instrumental analysis of pharmaceutical raw materials, in-process samples, and finished products. This role ensures all testing and documentation strictly adhere to
cGMP
and
GLP
standards.
Key Responsibilities:
Perform chemical testing using
HPLC, GC, UV Spectrophotometer
, and wet analysis methods.
Record and maintain all analytical data meticulously according to standard operating procedures (SOPs).
Ensure the calibration and maintenance of QC laboratory instruments.
Report any
Out of Specification (OOS)
results promptly to management.
Required:
Must be a B.Pharma graduate and available for
immediate joining
.
Job Type: Full-time
Pay: ?15,000.00 - ?22,000.00 per month
Benefits:
Paid sick time
Paid time off
Work Location: In person
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