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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | Sales / BD |
| EmploymentType | Full-time |
1. Responsible for smooth functioning of all production activities.2. Responsible for On-Line entries in BMR and Equipment Logs.3. Responsible for production as per Approved Formula.4. Responsible for review of executed Batch manufacturing Record.5. Responsible for involving in Process validation & Equipment Qualification and cleaning validation activities.6. Responsible for identification of training needs and giving/ arranging training to subordinates related to technical and cGMP aspects.7. Responsible for preparation of SOPs.8. Responsible for making SAP entries.9. Responsible for handling of deviation, incident and change control in the area.10. Responsible for handling of investigations related to market complaints.11. Responsible for implementation of cGMP standards and SOP compliance.12. Responsible for indenting Change parts / spares and additional equipment procurement as and when required.13. Trouble shooting in unit operation as and when required.14. Responsible for outcome of product as per quality standards.15. Responsible for handling of manpower in a controlled way for better productivity.16. Responsible for maintaining all documents related to production area as per cGMP.17. Responsible for monitoring batch manufacturing process yields and rejections.18. Responsible for planning and organizing the manpower and resources to meet daily, weekly and monthly schedules.19. Responsible for handling of documentation, SOPs and calibration records.20. Responsible to perform any other activity as directed by Production Manager as and when required.PPIC Packing Material JD1. Responsible for requesting BMRs / BPRs based on the production plan and creation of process orders in SAP.2. Responsible for monitoring stocks both for commercial and exhibits.3. Responsible for tracking and updating the daily receipts.4. Responsible to follow up with WH, and resolve any issues to get the material inward without any delays on daily basis.5. Responsible for ensuring all materials approved to avoid any delays of manufacturing of commercial and exhibit batches.6. Responsible for tracking the daily dispensing with warehouse, as per the plan.7. Responsible for monitoring and reporting production plan vs. actual plan.8. Responsible for tracking the delays in production against the plan and alert the concerned department.9. Upon receipt of PO Copy from marketing through his counterpart, ensure the availability of BMRs / BPRs, if required coordinate with QA department and ensure the availability.10. Responsible for initiation of code to code transfer request note for semi-finished analysis.11. Responsible for indenting rubber stereos for batch packing.12. Responsible for preparation of SOPs.13. Responsible for preparing the exhibit batches planning based on the tech pack/packaging note.14. Responsible for initiation of repacking request notes based on the FG ware house requisition.15. Coordination with Packaging department for preparation of MPCs based on priority.16. Responsible for initiation of Deviation/Change control if required for smooth functioning of day to day production activities against the Planning.17. Responsible for perform any other activity as directed by Production In-Charge as and when required.,
Keyskills :
process validationequipment qualificationhisdocumentationsapcontinuous improvement facilitationsopchange controlwinning others overtraining needsdeliverylogisticsltdpacking materialbatch manufacturingcleaning validationmanufacturing pro