Overall responsibility of managing and monitoring all the manufacturing and packing activities of non-sterile and Sterile Products Department, Oral Liquid and Semi Solid departments with full compliance of cGMP including  Manage all the technical Tablets, Dry powder,Injections,Syrups, Suspension,capsules,Drops,Ointment and Cream. Responsibility of managing and monitoring of all kinds of production activities right from the production planning, scheduling,manufacturing,filling and of packaging of products having in compliance with all the cGMP regulations in all the sections of Non-sterile and Sterile Products Department . Development of new SOP's and up gradation of existing SOP's and other related documents and production formats, manufacturing and packing procedures, qualification and validation documents and all other type of documentations and their upgrading. Multi-disciplinary professional with 14 years of impressive track record in the field of production of Non-sterile and Sterile, Liquid & Solids operations management in multinational environment, having desire to get challenging position in upper level management position with responsibilities including sound planning, problem solving with absolute honesty and total professional commitment.  Responsible of Planning, coordination and control of respective production resources to effectively achieve the set production targets & quality standards. and operational activities during manufacturing and filling of products, in process testing and packing operations as per cGMP, standards.  Responsible to ensure cost effective utilization of resources.

1. Overall responsibilityof managingandmonitoringall the manufacturingandpackingactivitiesof non-
sterile and Sterile ProductsDepartment,Oral LiquidandSemi Soliddepartmentswithfull compliance of
cGMP including
 Manage all the technical Tablets,Drypowder,Injections,Syrups,Suspension,capsules,Drops,Ointment
and Cream.
Responsibilityof managingandmonitoringof all kindsof productionactivitiesrightfromthe production
planning,scheduling,manufacturing,fillingandof packagingof productshavingincompliance withall
the cGMP regulationsinall the sectionsof Non-sterileand Sterile ProductsDepartment.
Developmentof newSOP'sandupgradationof existingSOP'sandotherrelateddocumentsand
productionformats,manufacturingandpackingprocedures,qualificationandvalidationdocumentsand
all othertype of documentationsandtheirupgrading.
Multi-disciplinaryprofessional with14 yearsof impressive trackrecordinthe fieldof productionof
Non-sterile andSterile,Liquid &Solidsoperationsmanagementinmultinationalenvironment,having
desire togetchallengingpositioninupperlevelmanagementpositionwithresponsibilitiesincluding
soundplanning,problemsolvingwithabsolute honestyandtotal professionalcommitment.
 Responsible of Planning, coordination and control of respective production resources to
effectively achieve the set production targets & quality standards.
and operational activities during manufacturing and filling of products, in process testing and
packing operations as per cGMP, standards.
 Responsible to ensure cost effective utilization of resources.
Major Responsibilities:
1.Responsible to Contribute to all aspects of production.
2. Develop and Review the drug manufacturing process
3.Coordinate Plant Maintenance operations with Plant Manager in various parallel activities,
such as warehousing, quality control and production towards the accomplishment of company
objectives.
4. Investigates new drugs and control the quality of drug products during production. This
ensures that new drugs meet standards of potency, purity, uniformity, stability and safety.
5.Responsible for developing informational materials concerning the uses and properties of
particular drugs and for evaluating the labeling, packaging and advertising of drug products.
6. To maintain good human relations by ensuring satisfactory working environment.
7.Responsible for the safely good housekeeping and environmental conditions and cleanliness of
plant and social area.

2. 8. Responsible for conducting training form Production personnel and ongoing training of
existing staff.
9.Directly responsible for the professional & managerial standard of officers and supervisors of
Production, ensuring all of them staff receive clear and consistent instructions and are motivated
to achieve the required output and ensure the establish line management.
10. To prepare daily/ weekly & monthly Production schedule in coordination with Material
Management department to ensure efficient & economic use of men power & equipment.
11. To supervise day to day Production operations.
12. To ensure production according to planed output, supply schedule and high standard of
quality.
13. To ensure thorough completion of necessary documents and records
14. To propose new ideas for process improvement and deal with all technical problems in
consultation with lateral associates where necessary.
15. To identify and highlight area of poor prime cost performance, and to propose appropriate
remedial action for improvement of prime cost performance.
16. To analyze down time and liaise with Engineering section for appropriate actions and ensure
efficient running of production machinery and associated equipment with regard to preventive
maintenance services.
17. To assist if necessary in success full implementation of new projects from proposal to
production. To provide assistance to R&D in scaling up of products