Manager - Production - IPCA Laboratories Limited - Ratlam (M.P.)
(1994-06 - 2025-10)
Ipca Laboratories Limited was established in the year 1975, having annual turnover of more than 3000 crores. It has manufacturing facilities for API and Intermediates, Formulation CRAMS and R & D at various locations in India. Exports its products in more than 100 countries around the world and high Brand equity in the domestic market. Ratlam unit is one of the biggest set-up Having Bulk Drugs & Formulations facilities with more then 2000 employees.
- Preparation, execution and completion of Production Schedules related to Production Targets.
- All RMs, Solvents & Finished Goods Inventory Control.
- Manpower planning, training, Shift Planning.
- Handling all manufacturing activities of commercial manufacturing Plant
- Coordination with Quality Assurance Dept. for optimization & execution of validation activities for all batches.
- Communication with QC, Maintenance, HR & EHS departments R&D to move the work ahead smoothly
- Training for Operators and Subordinates for making better work environment and safe practices.
- Improvement and Updating of Housekeeping of Plant Process Area, Documentation systems and Clean Area Practices.
- Handling change controls, deviation controls.
- Review and execution of Process & Cleaning Validation for different products.
- Maintain Good Documentation Practices
- To ensure safe process going on in plant.
- Individual responsible for the entire operation of plant to meet the target achievement, quality product, inventory management and maintain the predefined norms.
- Evaluation of current capacities and utilization rates against the business requirements.
- Resolve/ escalate concerns (OOS, OOT, RM issues) in discussion with respective/ concerned departments.
- To minimize the production cost through reduced time cycle
- Handling the audit processes with plant production and cross functional teams for relevant audits (Regulatory and customer audit) and preparation of compliance / observations report from all relevant audits.
