Job Description

Perform sampling, testing, and analysis of raw materials, in-process materials, and finished products as per approved specifications and standard operating procedures (SOPs). Operate and maintain laboratory instruments like HPLC, UV-Vis Spectrophotometer, pH meter, etc. Prepare and maintain test reports, logbooks, and relevant documentation to ensure compliance with cGMP and regulatory standards. Ensure timely calibration and maintenance of laboratory equipment. Conduct stability studies and support method development and validation as required. Ensure adherence to Good Laboratory Practices (GLP) and safety protocols in the laboratory. Support internal and external audits by regulatory agencies and clients. Identify and report any non-conformities or deviations, and participate in corrective and preventive action processes (CAPA). Co-ordinate with production, warehouse, and other departments for smooth workflow and material release.

Required Qualifications:

B.Sc. / B. Pharma / M. Pharma (Chemistry, Pharmaceutical Sciences, or related field). 1 to 3 years of experience in Quality Control in a pharmaceutical / veterinary pharmaceutical manufacturing setup. Knowledge of cGMP, GLP, and regulatory guidelines (WHO, GMP, ISO, etc.). Hands-on experience with basic laboratory instruments and analytical techniques. Strong documentation, observation, and reporting skills.
Job Types: Full-time, Permanent

Pay: ?20,059.07 - ?26,000.00 per month

Benefits:

Cell phone reimbursement Food provided Health insurance Internet reimbursement Provident Fund
Work Location: In person