Title: Production Executive
Carrying out manufacturing operations in compliance with current Good Manufacturing Practices, Good Documentation Practices and Data Integrity policy |
Ensure readiness of the facility at all times. |
Follow safety and hygiene policy as per the company norms. |
Ensuring the manufacturing/ Water treatment plant operations in compliance with current Good Manufacturing Practices, Good Documentation Practices and Data Integrity policy. |
Ensure readiness of the facility at all times. |
Online documentation during batch execution, ensuring documents and annexures are filled and maintained online. |
Weekly planning of production activities in coordination with production planner. |
Ensure packing & dispatch for products is carried out as per schedule. |
Preparation of monthly production report in PPT & submit to site head |
Monitoring and Maintaining of all WTP related operations and documents. |
Ensure the availability of required raw materials and consumables for WTP operations. |
Ensuring of WTP operation as per the SOP & safety instructions are followed in the shop floor. |
Adhering to Good Manufacturing Practices. |
Preparation of manufacturing documents & Checklists |
Assigning of LMS training and follow up with team for completion |
Updating the production team attendance in SAP as per the shift schedule |
Following the Standard Operating Procedures, Safety, Health and Environment measures. |
Ensure equipment PM & Instrument calibration are within the due date by coordinating with EAM team. |
Calibration check of instruments like pH meter and weighing balance in production |
Checking the readiness of equipment to initiate/ execute manufacturing activity. |
Ensure the cleanliness of raw material and packing materials before bringing inside the plant. |
Raw material, packing material receipt and check w.r.t BMR and issue slip with appropriate label. |
Ensuring the cleanliness of working area at all times. |
Monitor and control the production operations as per the batch manufacturing records. |
Co-ordinating with project team, consultants and internal cross-functional teams during the qualification activities |
Ensuring the availability of consumables like filter cloth, sample bottles, labels, filter cartridges for current and next shift. |
Carry out batch charging /filtration / Work up/ Drying activities as per the batch manufacturing record, and product handling and packaging |
Operate the DCS as per process requirements mentioned in the batch manufacturing record and online updation of the operations in the batch manufacturing record. |
Update and maintain the equipment logbook/ daily checklists. |
If any deviation/ variation is noted, inform immediately to supervisor for further proceedings. |
Non-conforming reports and corrective actions implementation in co-ordination with relevant team members. |
Cross checking the mother liquor, aqueous layer, spent solvent, spent solid and handover for disposal upon concurrence from shift in-charge. |
Sample submission to QC and preparation for next step. |
Handling of QMS Activities such as EQMS,EDMS |
Attendance update in SAP as per the shift schedule |
Updation of daily report and sharing with the team. |
Taking charge from previous shift after checking the reaction condition with the batch manufacturing record (BMR) and availability of equipment cleanliness checklist (ECC), raw material and solvent for the next operation. |
Completion of the operations within the BMR specified timings. |
Shift update to the superiors on the status of the project and plant status. |
Attendance of all training sessions assigned by the training coordinator /calendar. |
Effective performances by coordination with senior management. |
Cooperation with co-worker and focus on good relationship with all cross functional team. |
Follow good hygienic practices. |
Attending the training on the Standard operating procedure and other new topics to enriches knowledge. |
Ensure good teamwork by maintaining good relationship with subordinates. |
Preparation and execution of qualification documents like URS, SLIA, CLIA, RTM, DQR, RA, IQ, OQ, IOQ, PQ and QSR/VSR etc. |