Execute daily production activities in the injectable sterile aseptic manufacturing area as per batch manufacturing records BMRs and SOPs Monitor and ensure adherence to cGMP practices cleanroom discipline and aseptic techniques during manufacturing processes Operate and supervise machines like autoclaves vial washing filling sealing and lyophilization if applicable Coordinate with QA QC engineering and warehouse teams for smooth batch execution Maintain records and documentation - BMR logbooks calibration cleaning records and other regulatory documentation Perform line clearance and ensure availability of materials equipment and utilities before batch start-up Participate in deviation handling change controls CAPA and other quality-related investigations Ensure timely reporting of production data and support audits internal and external Train and guide operators and workers on SOPs GMP safety and hygiene standards Required Skills and Competencies Sound understanding of sterile aseptic injectable manufacturing processes Knowledge of GMP GDP cleanroom classifications and regulatory compliance WHO GMP EU-GMP MHRA USFDA Ability to operate and troubleshoot injectable equipment Positive documentation and communication skills Attention to detail discipline and teamwork attitude Preferred Experience Prior experience in a regulated injectable manufacturing facility SVP or LVP Job Type Full-time Pay 25 000 00 - 30 000 00 per month Schedule Day shift Work Location In person