Supervises vial manufacturing activities, including dispensing, washing, sterilization, and filling. Manages online documentation for logbooks, BMRs, and BPRs. Executes change controls via TrackWise and updates SOPs, URS, and Quality Risk Assessments to ensure regulatory compliance.
B.Pharm. degree of a recognised University or equivalent. experience in a reputed Pharmaceutical concern. Govt. undertaking or Hospital having more than 500 beds, of manufacturing medicines/drugs and supervision of Pharmacy Service. Goa Public Service Commission
Maintain equipment logbooks, calibration records, and analytical test data sheets. Preparation and qualification of working standards, reference standards, and primary standards.
Hiring dynamic and self-motivated individuals to work in our Production Department, focusing on manufacturing pharmaceutical products in compliance with quality and safety standards.
Support purification activities such as column chromatography, extraction and filtration. Record experimental details in laboratory notebooks or an electronic laboratory notebook.