Handling of all activity applicable for manufacturing of drugs.
2. Implementation and control the production schedule.
3. Review and adjust the schedule where needed.
4. Determine and improvements to the production process.
5. Management of manpower in the organization.
6. Technical training of manufacturing chemist about cGMP and International Standard of
Quality Management.
7. Ensure efficient collaboration and co-ordination between relevant departments including
procurement, distribution and management.
8. Ensure revision of document according tocGMP&WHO norms.
9. Internal audits and their compilation.
10. Handling of devation/incidence.
11. Handling of investigation on various stages.
12. Direct reporting to Managing Director ().
Control the production as dispatch schedule with quality productivity and process control of
product.
Monitor and control and correct all critical parameters at all stages of production. Ensure proper
utilization of resources.
Ensure product storage as per WHO & Other International regulatory guidelines and others
practices. Ensure in-process control and strict implementation.
Ensure proper consumption of Raw and Packing material up to final yield of the product.
Packing Material developmentas per change part application - Tablet/Capsule/Liquid,Product
development SR tablet, coated, uncoated& dispersible tablets and capsule& Oral Liquid, Dry
Syrup,B-Lactum product.
Experience : 10 - 17 Years
No. of Openings : 2
Education : B.Pharma, M.Pharma, M.Sc
Role : Production Manager
Industry Type : Manufacturing / Production / Quality
Gender : Male
Job Country : India
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