Cadila Pharma

"•	Ensure the cGMP Compliance and schedule M compliance in production.
•	Ensure the proper utilization of men and machine of Granulation area.
•	Ensure the training of production staff and worker.
•	Ensure the development progress periodically of personals and take necessary corrective action.
•	To lead the Granulation department with respect to developing the second line.
•	To ensure the delivery of products as per the production target.
•	To ensure and monitoring yield, Wastage, WIP & operation expenses of Granulation area.
•	To co-ordinate with tablet sub- department, Quality Assurance, Quality Control and engineering department to achieve production delivery as per production schedule.
•	To ensure daily production report and submit to higher management.
•	To ensure periodic qualification of equipment and process validation are carried out as per schedule.
•	Raise the change control for new equipments installation and completed the I.Q, O.Q and P.Q of new equipments.
•	Raise the deviation for unplanned or any incident base activity performed related to process, quality or any other.
•	Performing a SAP entry related to manufacturing area and prepare a Purchase indent in SAP. 
•	To ensure execution of new product / ANDA product as per schedule.
•	To ensure the maintenance of production building and premises.
•	Batch Manufacturing Record review and release for next stage.
•	To Review SOPs/BMRs & Qualification protocol and reports.
•	To ensure implementation of quality policy in Granulation area.
•	To ensure the training & development of people.
•	To ensure the cost effective improvement & measure to control expenses.
•	To ensure the preventive maintenance of equipment and departmental documents as per regulatory requirement for Granulation area.  
•	To ensure the quality of the product and involvement in complaint investigation.
•	To ensure the work discipline and cleanliness in production area and maintain all time readiness of Granulation area for regulatory/external and internal audit.
•	To prepare Standard Operating Procedure.
•	Handling of deviation, initiation of change control and CAPA.
•	Any other job described by department/production/unit head."

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