Housekeeping of the warehouse & maintaining the required temperature Verification of weighing equipment Preparation of purchase requisition slip and handling it over to purchase officer Supervision of loading of material as per delivery challan Planning of raw materials as per the requisition slip received from all the plants Supervision of loading of material as per delivery challan. Communication of raw material received schedule to Production Managers and ensure adherence to the schedule. Issuing raw materials as per raw material requisition slip from the production department Issuing raw materials as per FIFO system Coordinating for the warehouse maintenance with the Engineering department Maintaining required documentation for ISO and GMP

Housekeeping of the warehouse & maintaining the required temperature Verification of weighing equipment Preparation of purchase requisition slip and handling it over to purchase officer Supervision of loading of material as per delivery challan Planning of raw materials as per the requisition slip received from all the plants Supervision of loading of material as per delivery challan. Communication of raw material received schedule to Production Managers and ensure adherence to the schedule. Issuing raw materials as per raw material requisition slip from the production department Issuing raw materials as per FIFO system Coordinating for the warehouse maintenance with the Engineering department Maintaining required documentation for ISO and GMP

To prepare Standard Operating Procedures of all departments. To review batch manufacturing records protocols and reports of all Active Pharmaceuticals Ingredients and Intermediates to support DMF / FILING. Follow quality assurance systems as per cGMP guidelines. To ensure that all manufacturing operations at the location comply with ICH Q7 system, documentation and records. To follow a system for releasing or rejecting all APIs. To follow up a system for releasing or rejecting intermediates for use outside the control of the manufacturing company. To follow a system to release or reject RM, Intermediates, packing and labeling materials. To perform product quality review. To prepare product labels and establish a system to control issuance of labels. To review raw data of analysis before release of the batch. To support Asst. Manager / Officer for Q.A activities like qualification, validation, calibration, and area monitoring. To prepare documents for customer questionnaires and support. To prepare, review and respond to the Regulatory Query. To fill the customer vendor questionnaire as per customer requirement & provide VQ related declaration. To prepare & review the DMF as per the pharmacopeia & customer requirement. To Submit the DMF to the Regulatory Authority as per the Regulatory requirement. To prepare & review declaration as per customer vendor questionnaire requirement. To perform Nitrosamine risk assessment as per the guideline requirement. To perform Genotoxic risk assessment as per the guideline requirement.

Housekeeping of the R & D area and maintaining all apparatus related to experiment. Verification of weighing equipment. Validation experiment carried out on a related project. Manufacturing the products as per R&D trials. To develop the process as per ICH / pharmacopoeia quality. To optimize the finalized process and scale-up. To generate the negative and challenging data required to meet the scale up challenges. Verification batch and validation batches. Coordination with the ADL department. Coordinate work with lab peers. To maintain a lab notebook of all current projects. To check and review the calibration record of the instruments / equipment. To take safety awareness related to hazardous reactions. Give reporting to the department head as per timeline.

To carry out the preventive maintenance of utilities and plant equipment & co-ordinates with concern department as per preventive maintenance schedule To check, verify and maintain record of operational and maintenance documents of all equipment as per GMP norms . To maintain the parameters of HVAC system as per norms/SOPs etc. To maintain record of operational and maintenance documents of HVAC system and all utilities as per GMP norms . To attend the break down maintenance of utilities & plant equipment and minimize break down time. To maintain necessary documents with respect to machine history card. To follow the all safety equipment during work. To maintain the daily log sheet of all utility equipment To carry out the proper spare during the maintenance. To participates in execution of calibration, qualification and validation activity of area, equipment and process related to utility. To maintain the all utility area cleaning. To participates in training program. To follow the work permit system as per SOP To maintain the all material in / out procedure. To good communicate with other colleagues