Perform sampling and analysis of raw materials, in-process samples, finished products, and packaging materials.
Conduct physical, chemical, and instrumental testing as per SOP.
Instrument Operation
Operate and calibrate analytical instruments like
HPLC, GC, UV, IR, Dissolution Tester, pH Meter
, etc.
Maintain instrument logs and calibration records.
Documentation
Prepare and review test reports, COA, logbooks, and analytical records.
Ensure all documentation is recorded as per
GLP, cGMP, and FDA
guidelines.
Quality Compliance
Follow SOPs, GMP, and regulatory guidelines strictly.
Report deviations, OOS (Out of Specification), OOT (Out of Trend), and maintain CAPA records.
Stability Studies
Conduct stability sample analysis and maintain stability logs.
Support validation and verification activities when required.
Coordination
Coordinate with production, QA, and R&D teams for smooth workflow.
Assist during audits (internal & external).
Safety & Hygiene
Follow laboratory safety procedures and maintain a clean working environment.
Ensure proper handling and storage of chemicals.
Skills Required:
Strong knowledge of
GMP, GLP, WHO, FDA, and ICH guidelines
.
Hands-on experience with pharma analytical instruments.
Good documentation and reporting skills.
Ability to handle multiple tasks and meet timelines.
Strong attention to detail and accuracy.
Qualification:
B.Pharma / M.Pharma / B.Sc / M.Sc (Chemistry or relevant stream).
Prior QC experience in a pharmaceutical company preferred.
Job Type: Permanent
Pay: ₹18,000.00 - ₹22,000.00 per month
Benefits:
Provident Fund
Work Location: In person
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