19 Aug
|
Cadila Pharmaceuticals
|
Dholka
19 Aug
Cadila Pharmaceuticals
Dholka
- 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 recent 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.
📌 Executive (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka