Qc Executive

Role & responsibilities

• Perform sampling and testing of raw materials as per approved specifications and SOPs.
• Conduct chemical and physical analysis of raw materials using applicable pharmacopoeial methods.
• Perform testing as per IP, BP, USP, Ph. Eur. and approved in-house specifications.
• Operate and maintain laboratory instruments such as HPLC, GC, UV, IR, pH meter, analytical balance, and other QC instruments, as applicable.
• Review test results and ensure compliance with approved specifications.
• Prepare and maintain raw material test reports, analytical worksheets, and laboratory records.
• Ensure proper documentation in accordance with GMP/GLP and data integrity requirements.
• Handle OOS, OOT, deviations, and laboratory investigations as required.
• Coordinate with QA, Warehouse, and other departments for timely release/rejection of raw materials.
• Ensure proper handling, storage, labeling, and disposal of laboratory samples.
• Follow laboratory safety procedures and maintain cleanliness and housekeeping standards.
• Support method validation, method verification, instrument calibration, and laboratory activities as required.

Preferred candidate profile

We are looking for a QC professional responsible for testing and analysis of pharmaceutical raw materials as per approved specifications, SOPs, pharmacopoeial standards, and GMP requirements.