- Plans/Schedules for manufacturing (processing) activities across the month over various lines along with execution of manufacturing (processing) activities of Non-sterile department.

- Ensures, on regular basis, that all the processing and packing lines should run in conformance to cGMP standards.

- Follows the regulation of various agencies (USFDA, TGA, MHRA, MPA, WHO, Schedule M etc.).

- Conducts Departmental meeting A two-way communication process for reviewing various points for improvement in the department.

- Participate in validation activities, tech transfer activities as per the protocol.

- Training to subordinate to improve process related practices and documentation.

- Counsels erring workmen in case discrepancy are found in output based on machine speed verses run time.

- Monitors shop floor NCs by counselling of erring workmen and display on notice board, initiate disciplinary action.

- Monitors on regular basis parameters having financial impact like yield, packing material consumption, operational lead time, labor utilization and take measure for continuous optimization/improvement.

- Review of various RFPs (Request for Proposal) from customers and preparing Gap analysis.

- Participate in various customer calls and provide inputs.

- Involve in various Regulatory, Customer and Internal audits.

- Ensures no shortfall in supply to market.



Take care of sharp fluctuations like sudden demand spikes.

- Follow the GDP and reviews various reports/ records of the department.

- Sets objectives (Annual) for individual repetitions and monitors the progress. Gives periodic feedback regarding performance. Guides whenever necessary in case of difficulty in execution of any objective.

- Conducts final performance reviews sitting with individuals’ representatives along with the HOD and sends the reports to personnel dept. Recommends for performance grades for each reportees.

- Suggest and implement various cost optimization/de-bottlenecking projects.

- Helps in line setting for current products with new pack profile.

- Helps in investigating market complaints.

- Review and approve the Batch Processing records (BMR) and other quality documents.

- Involvement in various Capex and Opex finalization.

- Budget preparation and Manpower planning.

- Prepares capital investment requisitions for any new product/modification of existing facility.

- Takes up the responsibilities of the immediate superior in his absence.

- Approve new SOP and existing SOP’s after updation.

- Initiate / Review/ Approve Change controls and Deviations, CAPA, Change controls in electronic system as per the need.

📌 Associate General Manager - Production (Formulation) (Pithampur)
🏢 PIRAMAL PHARMA
📍 Pithampur