Shift In charge - Granulation

• Execute manufacturing activities as per production plan, SOPs, BMRs, and cGMP requirements.
• Raise process orders in SAP and maintain production documentation.
• Monitor equipment operation, line clearance, environmental controls, and manpower allocation.
• Review BMRs, logbooks, cleaning records, and production-related documents.
• Handle QMS activities such as Deviations, Change Controls, CAPA, Investigations, and Compliance.
• Support validation, qualification, calibration, and preventive maintenance activities.
• Ensure batch reconciliation, yield control, and process monitoring.
• Participate in regulatory audits and inspections (USFDA, MHRA, EU-GMP, WHO-GMP).
• Maintain EHS compliance and conduct training for shop-floor personnel.
• Drive continuous improvement, productivity enhancement, and data integrity compliance.

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc / B.E. (Chemical)

Experience: 3-8 Years in Pharmaceutical Manufacturing (OSD/Sterile/API preferred)