Senior Executive

Cadila Pharmaceuticals Limited; Ankleshwar; Sur place; INR 300 000 - 450 000; Plein temps

Résumé du poste

Cadila Pharmaceuticals Limited is seeking a Manufacturing Operator to execute operations per BMR, SOPs and production plans, while supervising shift activities to ensure timely batch completion.

The role involves handling chemical processes including crystallization, filtration, drying, milling, blending and packing, monitoring process parameters, maintaining GDP-compliant records, and coordinating with QA, QC, Engineering, Warehouse, EHS and Maintenance for smooth manufacturing operations.

Responsabilités

• Execute manufacturing operations per approved Batch Manufacturing Records (BMR), SOPs, and production plans.
• Supervise shift activities and ensure timely completion of production batches.
• Handle chemical reactions, crystallization, filtration, drying, milling, blending, and packing activities.
• Monitor critical process parameters and ensure compliance with process specifications.
• Ensure line clearance, equipment cleaning, and status labeling before batch initiation.
• Review and complete BMRs, logbooks, equipment records, and production documentation following GDP.
• Coordinate with QA, QC, Engineering, Warehouse, EHS, and Maintenance for smooth operations.
• Investigate deviations, incidents, OOS/OOT observations, and implement CAPA with QA.
• Ensure compliance with cGMP, Data Integrity, EHS guidelines, and regulatory requirements.
• Optimize process yield, reduce cycle time, minimize solvent consumption, and improve productivity.
• Monitor utility consumption and ensure effective utilization of manpower and equipment.

Description du poste

Job Description:

Execute manufacturing operations as per approved Batch Manufacturing Records (BMR), SOPs, and production plans. Supervise shift activities and ensure timely completion of production batches. Handle chemical reactions, crystallization, filtration, drying, milling, blending, and packing activities. Monitor critical process parameters and ensure compliance with process specifications. Ensure line clearance, equipment cleaning, and status labeling before batch initiation. Review and complete BMRs, logbooks, equipment records, and production documentation following Good Documentation Practices (GDP). Coordinate with QA, QC, Engineering, Warehouse, EHS, and Maintenance for smooth manufacturing operations. Investigate deviations, incidents, OOS/OOT observations, and implement CAPA in coordination with QA. Ensure compliance with cGMP, Data Integrity, EHS guidelines, and regulatory requirements. Optimize process yield, reduce cycle time, minimize solvent consumption, and improve productivity. Monitor utility consumption and ensure effective utilization of manpower and equipment.

Requirements: