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Job description

Role & responsibilities: • Operate and maintain equipment such as Viswill Camera Inspection, Fette Compression, Sejong Compression, granulation systems, capsule filling machines (AF 90 T), auto coaters, and tablet printing machines. • Complete and review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) in real time to ensure data integrity and compliance with cGMP. • Conduct in-process quality checks on tablets, including weight variation, hardness, thickness, and moisture content, etc. • Ensure documentation is completed in accordance with Good Documentation Practices (GDP). • Perform line clearance and equipment/area cleaning to prevent cross-contamination. • Apply mechanical aptitude to troubleshoot machinery and understand different tablet tooling. • Adhere strictly to established safety procedures without deviation. Preferred candidate profile Qualification: ITI / HSC / SSC Experience: 25 years in the pharmaceutical industry (preferably OSD plant experience)

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