Job Summary:
We are looking for a detail-oriented Quality Control Executive to perform chemical and instrumental analysis of raw materials, in-process samples, finished products, and stability samples. The ideal candidate will ensure compliance with cGMP, GLP, and regulatory requirements while maintaining accurate laboratory documentation.
Key Responsibilities
- Perform testing of raw materials, in-process, finished products, and stability samples.
- Operate HPLC, UV, Dissolution, FTIR, and other QC instruments.
- Prepare and maintain analytical reports, COAs, and laboratory documentation.
- Ensure compliance with cGMP, GLP, and data integrity requirements.
- Investigate OOS/OOT results and support CAPA activities.
- Perform calibration and routine maintenance of laboratory equipment.
- Assist in method validation, stability studies, and regulatory audits.
- Coordinate with QA and Production for timely product release.
Qualification
B.Pharm / M.Pharm / M.Sc. (Chemistry)
Experience
3–5 Years in a Pharmaceutical Formulation Manufacturing Plant.
Pay: ₹15,000.00 - ₹35,000.00 per month
Work Location: In person
