Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the production of high-quality injectable pharmaceutical products Essential Functions: • To ensure cGMP and compliance review in the manufacturing shop floor and packing areas. • To supervision of dispensing activity of manufacturing shop floor and packing areas. • To Issuance of Bottle label, Ouster and Medication guide for commercial batch. • Rsponsible for providing machine and area clearance. • To conduct Sampling of reserve sample, stability sample and In-process checks during execution of batch packaging as per Batch Packaging Record (BPR) and stability study protocol. • Online Documents and records review like equipment’s logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records etc.. • Calibration of IPQA instruments. Additional Responsibilities: • Real-time Monitoring and Compliance Reporting. • Participation in Investigations. • Provide on-the-job training to shop floor personnel on GMP practices, quality standards, and documentation practices. • Maintain IPQA-related documents and records in a state of audit readiness. • To have good written and verbal communication skills in English language. Education: • Bachelors Degree (BA/BS) B. Pharm - Required • Master Degree (MS/MA) M. Pharm - Preferred Experience: • 2 - 4 Years