Deputy Manager Job in Cadila Pharmaceuticals Ltd at Jammu

Job description:- To ensure that GDP &cGMP practices shall be followed from the premises to their section. To follow the all respective SOPs & BMR procedure in the department during operation. Ensure the activity perform as per MMD-I. To ensure balances should be calibrated and verified as per SOP before operation. To ensure all batches are dispensed and quantity to be verified as per BMR. Setting up production targets and achieve the same within time in granulation area. To review Daily Production & Packing plan for the Softgel & Hospicon Products. To check and ensure dispensed batches for the day in advance. To keep the area all time ready in line with c-GMP requirement. To follow manufacturing & Packing of product as per the respective BMR/BPR. To follow up with maintenance personal for solving engineering related issues and keep follow up with the maintenance for on time rectification of break down. Principal Tasks:- To maintain quality and productivity. To ensure that Zero accident & Zero tolerance in the area. To ensure all respective SOPs, BMR/BPR Procedure & Discipline in the department & Operation. Responsibilities:- To follow proper Gowning / De-gowning procedure as per SOP. To do the work allocation properly to workmen based on their competency to meet the daily production plan. Check and ensure that they are properly gowned and protected for the assigned work. To keep the daily basis tracking for productivity of Manpower and Machines. To check and ensure that all equipment’s used in the dept. are validated and their instruments are calibrated including the balances, ensure their cleanliness for use in good condition. To ensure the area and Equipment Cleanliness & Environmental Condition suitability and in-process checks to be carried out properly before startup and during batch manufacturing. To prepare the investigation report, fill online deviations if any, and other quality document like change Controls, CAPA wherever necessary for the strengthening of quality systems. To monitor the yield of every Products, stage wise on daily basis. Participate in resolving the issues in the CFT being a team member, and a functional representative of the CFT. To ensure processes needed for integrated management system for establishing, implementing and maintaining properly for your own department. To participate in periodic IMS system audits and maintains the records. To participate in training for internal auditors for IMS System to participate in various Awareness trainings on Environment, Health and Safety. To interact with the cross functional team (QA/QC/RM/PM/ENGG) for all technical and non-technical issue and resolve the same timely without affecting the product quality and delivery. Co-ordinate with Maintenance personal regarding breakdown and preventive maintenance of equipment’s or facility. Give necessary instructions to the operators & supervisor for production & Packing activities effectively. Inform to superiors of any breakdowns, Deviations, HR issues & productivity issues. Prepare and submit daily reports as required. Check and ensure that all SAP related entries completed on-line