Production Manager/ Pharma Company (Raichur)

1. <\/span> <\/span> <\/span>Responsible for indenting, approving and receiving of batch production records, cleaning records and packing records as per production requirement.<\/span> <\/p> 2. <\/span> <\/span> <\/span>Responsible for raise the raw material indent and approving of indented raw materials as per production planning.<\/span> <\/p> 3. <\/span> <\/span> <\/span>Responsible for Maintain positive Housekeeping in the plant environment.<\/span> <\/p> 4. <\/span> <\/span> <\/span>Responsible for to coordinate cross functional team to execution the plant operations smoothly.<\/span> <\/p> 5. <\/span> <\/span> <\/span>Responsible for monitoring the equipment utilization and manpower distribution for effective utilization.<\/span> <\/p> 6. <\/span> <\/span> <\/span>Responsible for initiation, review and approve the indents i.e., procuring production needs to run smooth production.<\/span> <\/p> 7. <\/span> <\/span> <\/span>Responsible for monitor all the schedules implementation (Production planning, Preventive maintenance, calibration etc.)<\/span> <\/p> 8. <\/span> <\/span> <\/span>To ensure the compliance of production activities.<\/span> <\/p> 9. <\/span> <\/span> <\/span>Responsible for production planning and meet the target time lines.<\/span> <\/p> 10. <\/span> <\/span> <\/span>To monitor and close the QMS documents.<\/span> <\/p> 11. <\/span> <\/span> <\/span>To involve / participate in Internal Audits.<\/span> <\/p> 12. <\/span> <\/span> <\/span>To extend support for customer audits / regulatory audits.<\/span> <\/p> 13. <\/span> <\/span> <\/span>To involve qualification activity.<\/span> <\/p> 14. <\/span> <\/span> <\/span>To give training to shop floor team.<\/span> <\/p> 15. <\/span> <\/span> <\/span>To ensure the safety rules and regulations in the team during perform the work.<\/span> <\/p> 16. <\/span> <\/span> <\/span>Attending training programs (GMP, job training & safety) as per the schedule.<\/span> <\/p> 17. <\/span> <\/span> <\/span>Review of completed batch production records, equipment log book and shift handover log book regularly.<\/span> <\/p> 18. <\/span> <\/span> <\/span>To monitor the online BPR entries and new products training before execution of the batch.<\/span> <\/p> 19. <\/span> <\/span> <\/span>Responsible for preparation, review and approval of all controlled documents relating to the quality of API’s and intermediates. (Standard operating procedures, batch production records, forms, protocols, reports etc.).<\/span> <\/span> <\/p> 20. <\/span> <\/span> <\/span>Responsible for initiation, timely implementation, effectiveness and closure of QMS activities like change control, deviation, OOS, investigation and CAPA.<\/span> <\/p> 21. <\/span> <\/span> <\/span>Review of all type of validation protocols and reports including campaign reports.<\/span> <\/p> 22. <\/span> <\/span> <\/span>In the absence of immediate superior, shall be responsible for his activities.<\/span> <\/p> 23. <\/span> <\/span> <\/span>To perform any other activity assigned by the superior / Plant Head.<\/span> <\/p> <\/span> <\/p> <\/span> <\/p> <\/div> <\/span> Apply on Kit Job: kitjob.in/job/4lvayp