Production Manager
2 months ago
Job Title - Production Manager
Department - Pharmacy
Reports to - Division Head
Responsible for:
1. Production- planning – Plan the daily and weekly production schedule based on the details such as the pending orders for domestic and export, stock on hand, preparation status, last 6 months sales, etc2. Ensure Overall compliance of production activities3. Monitoring the overall production related activities such as sanitization of packing materials and production things, monitoring of clean rooms, bulk manufacturing, filtration and filling process, steam and dry heat sterilization, in process and final checking, packing, finished goods storage and shipping process.4. Production man power planning to achieve the target5. Reduce the rejection rate and improve the yield6. Takes control over the incoming Raw material, packing material and stock maintenance depends on schedule and marketing forecast.7. Responsible for maintaining the inventory ratio at the rate of below 3.1%.8. Follow up with suppliers to get the material on time so as to avoid production delays.9. Follow up and track the invoices, material and shipment of inward material with support of Material controller.10. Ensuring overall training of the production staffs with respect to production related process.11. Perform the internal quality audit for other division as per audit schedule as auditor, and also attending the internal and external quality audit for our division as auditee.12. Co - ordinate with QA Manager for taking any corrective action related to production, quality and customer service.13. Coordinate with QA manager for approving the vendors.
Authority For:
1. Cleanroom validation – ISO14644 part I, Part II and III2. Packaging validation – ISO 11607 part I, Part II3. Sterilizer validation ( Steam/dry heat) – 17655-I,4. Cleaning validation – As per GMP5. Media fill validation – ISO 134086. Visual inspection validation,7. New equipment qualification & validation8. Production process validation9. Maintaining all production related documents, SOP and validation documents.10. Approving all quality documents pertaining to production.11. Co ordinate with R&D for introducing and developing new product, process related to production.12. Scheduling production plan for new development product filling.
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