Application for production

Avatar of Venkateswarareddy.
Avatar of Venkateswarareddy.

Application for production

Assistant manager production @ Jubilant generics LTD
Hyderabad, Telangana, India
JOB DESCREPTION: Execution of production through Distributed control system (DCS) through SIMMENS (softwarePCS 7) Planning and execution of batches as R&D requirement. Involving Scale up of the products from R&D to plant. Effective participation in technology transfer of new drugs coming from R&D. Resetting & Resolve process problems. Execution the batches without deviating the production schedule. Handling of multi products in manufacturing area Ensuring the data integrity compliance, and giving training to persons. Strict adherence of production targets to right time with consistency in yield and quality. Controlling and updating the records of process as per SOP’s. Creating pleasant working condition by maintaining good housekeeping and discipline. Ensuring personnel hygiene and health conditions as per sop, Monitoring critical process parameters and all operational norms. System strengthening by reducing deviations. Productivity improvement by optimum utilization of equipment and man power at all times. Maintaining the process equipments in good condition and support for timely preventive maintenance. Manufacturing the drug products as per Batch Production Record (BPR) and performing process operations as per standard operating procedures. Procuring raw materials from warehouse by raising a raw material requisition from based on the requirement Procuring raw materials from warehouse by raising a raw material requisition Through SAP and RM consumption and equipment closing Through SAP. Follow change control procedure in case of permanent changes and follow deviation (planned) new/changes in manufacturing equipment. Working with the cross functional teams like R&D, PD Lab, TSD, ESD, EHS, QC & QA for smooth functioning of the plant Generation of deviation reports in case of deviation from standards established and submits the completed deviation report to quality assurance department for verification and corrective action. Proper implementation of in-process sampling procedures
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Published: Nov 13th 2020
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