Manager Production

USV


Job Location:

Baddi - India

Monthly Salary: Not Disclosed
Posted on: 17 hours ago
Vacancies: 1 Vacancy

Job Summary

1. To check that production plan / schedule is followed.

2. To check that products are produced and stored as per batch record according to appropriate documentation in order to obtain the required product quality.

3. To check the compliance with the requirements of current good manufacturing practice (cGMP).

4. To review and sign production records.

5. To check the availability of raw/packing materials and production consumables.

6. To ensure that preventative and predictive maintenance of production equipment is carried out as per schedule.

7. To ensure that calibration of instruments in production department.

8. To prepare and review departmental SOP.

9. To maintain various production records with reference to man. machine and material.

10. Participate to carry out investigation with reference to lower yield and abnormalities in processing.

11. To ensure that required BMR/BPR and SOP are available in production department.

12. To give suggestions with reference to cost saving/productivity improvement in yield.

13. To impart the required initial and continuing training of production department personnel according to need.

14. To check that safety practices are followed in production department.

15. To verify the cycle time per product.

16. To carry out production scale up for new products in coordination with DDRL.

17. Responsible for minimizing down time of machine.

18. To calculate and arrange manpower according to production plan.

19. To ensure the online entry of data in SAP S/4 HANA a per current version of SOP No. JMF-SOP-0113 and SAP master data maintenance as per SOP no. JMF-SOP-0114.

20. To supervise validation activities.

21. Responsible for all EHS related compliance and implementation of safety regulations.

22. assist to carry out daily quality and safety talk.

23. Co-ordination with other function like QA QC Project Purchase warehouse HR Engg. Account and DDRL for smooth running of production plan.

24. To maintain management information sheet.

25. To ensure the implementation of monitoring CAPA.

26. To train the superior for compliance and productivity in area.

27. Training to subordinate to enhance their skill.

28. To build up the quality culture to improve the quality of products.

29. Self-audit/inspections to done as per annual schedule.

30. To carry out the investigation.

31. To carry out the GEMBA walk.

32. Manpower management and team alignment.

33. To be responsible to take follow up and give input & suggestion for quality and complaince monitoring - QMS elements ( Change control Deviation OOS OOT Incident CAPA complaints QRM etc.)

34. Management of related activities in various software at site i.e SAP elms TWD VLMS etc.

35. To execute the risk management activities in the production area by apply the risk management tool as as FEMA/Risk ranking & risk filtering techniques.

36. CAPA identification / implementation & effectiveness GLOBAL CAPA compliance.

37. To participate in self audit as self-auditor & to ensure the timely completion of compliance as per predefined timelines of self-audit/ QCMT audit/external audit ( customer/regulatory).

38. Ensure all time readiness for internal external regulatory audit customer audits. corporate quality audits and compliance.

39. Responsible for applicable trend review.

40. Site QRC discussion point response.

41. Responsible for escalation to higher management as per SOP matrix.

42. To monitoring of plant performance indicators.

43. To follow the statutory legal and safety compliance.

44. To ensure training and development of the people.

45. To ensure backup activity of equipments having facility for data storage.

46. To ensure audit trail for CSV equipment are performed.



Required Experience:

Manager

1. To check that production plan / schedule is followed.2. To check that products are produced and stored as per batch record according to appropriate documentation in order to obtain the required product quality.3. To check the compliance with the requirements of current good manufacturing practice...