Job Description

• 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.


Job Details

Role Level: Associate Work Type: Full-Time
Country: India City: Dholka ,Madhya Pradesh
Company Website: https://www.cadilapharma.com/ Job Function: Administrative Support
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


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