Satish Kumar Email & Phone Number

Hyderabad Area, India

 Execute the production operations in consultation with department heads. Ensure quality of Production  Understanding and implementing manufacturing strategy as per cGMP. Online documentation of Batch Manufacturing Records. Assisting production manager in day to day activities of production. Proper management of manpower Providing maximum production output in allotted shift.  Co-ordination with stores/Production superiors.  Monitor GMP in shop floor. Certify line clearance as per current procedures. Carry out inprocess checks as per GMP Interacting with engineering department abut validation or any repair of pharmaceutical equipments. Co-ordination between multiple departments to ensure smooth flow of all departments. Periodically training employees as peer current needs with respect to cGMP safety, health and hygine and other on-the-job training. Maintain all the documents of the department including SOPs, BMR and other day-to-day documents as well as online documentation of production activities Plan the production activities of the production department as per schedules & timely bond deliverieies.

Hyderabad Area, India

This Experience was help me a lot in which way means when we are studying time we don't know the practical knowledge on basic subject but now we know what is it and we get some idea on particular work so we have to improve my skills and knowledge with work with many organizations.

 Execute the production operations in consultation with department heads. Ensure quality of Production  Understanding and implementing manufacturing strategy as per cGMP. Online documentation of Batch Manufacturing Records. Assisting production manager in day to day activities of production. Proper management of manpower Providing maximum production output in allotted shift.  Co-ordination with stores/Production superiors.  Monitor GMP in shop floor. Certify line clearance as per current procedures. Carry out inprocess checks as per GMP Interacting with engineering department abut validation or any repair of pharmaceutical equipments. Co-ordination between multiple departments to ensure smooth flow of all departments. Periodically training employees as peer current needs with respect to cGMP safety, health and hygine and other on-the-job training. Maintain all the documents of the department including SOPs, BMR and other day-to-day documents as well as online documentation of production activities Plan the production activities of the production department as per schedules & timely bond deliverieies.

Balanagar, Hyderabad.

ÿ Monitoring the following process activities of Tablets Capsules & Dry syrupÿ Rechecking the grass weights of raw materials• Sifting raw materials• Mixing (Wet granulation & Dry Granulation)• Drying • Blending• Compression• Filling capsules• Filling of Dry syrup & Sachetsÿ Responsible For the Preparation of Batch Manufacturing Recoedsÿ Responsible For the Preparation of Equipment log Sheetsÿ Responsible For the Preparation Performance Qualification of The Equipmentÿ Responsible for checking of the parameters of the Tablets and Granules like:-• Disintegration• Friability• Moisture Content of the Dried Granulesÿ Responsible for ensuring the environmental conditions like (Temperature, Relative humidity & Differentiate Pressure) during in processHandling of Man Powerÿ