This role supports manufacturing operations for oral solid dosage (OSD) products by executing routine production activities in a regulated pharmaceutical environment. The role involves operating equipment used in granulation, blending, compression, and coating processes while adhering to batch manufacturing records and standard operating procedures. The incumbent handles raw materials, intermediates, and finished products with a focus on quality, safety, and compliance with cGMP requirements. It ensures accurate documentation of all manufacturing activities to maintain data integrity and traceability. The role contributes to efficient batch execution, supports equipment upkeep, and participates in continuous improvement initiatives to enhance product quality and operational efficiency.
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