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Technical Supervisor

Cadila Pharmaceuticals Ltd
Jammu, IND
Full-time
Entry · 2+ years experience
Onsite
INR 200000-500000 yearly / year
Discovered Today

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Major Purpose Of The Job:- To review Daily Packing plan for the assigned Packing line activities. To ensure that arrangement of dispensed batches for the day in advance. To ensure that Daily/Weekly/Monthly packing schedule as per plan. To packing and deliver the product on time which complies the regulatory requirement. To maintain cGMP norms in the department. To ensure that SOPs are followed in the department. To allot Job distribution to the staff and operator. To ensure optimum utilization of Man and Machine Hours. To carry out load down in-process checks during packing operation. To solve technical problems and suggest modification to improve productivity on day-to-day basis To check up with maintainance for solving Engineering related issues. To ensure and submit daily packing report. To ensure optimization of resources and reduction of waste/rejections. To review, investigate and corrective and preventive actions to maintain the product quality. Principal Tasks:- To maintain quality and productivity. To ensure that Zero accident & Zero tolerance in the area. To follow all respective SOPs, BPR Procedure & Discipline in the department & Operation. Responsibilities:- To ensure that work is allocates properly to workmen based on their competency to meet the Daily production plain. Check and ensure that they are properly gowned and protected for the assigned work. To follow the startup and closing timings of the machine. To arrange all Packaging materials for Coding and packing. To reduce interruption of down time. To follow the proper utilization of machines. To follow the achievement of daily targeted packing plan Reconcile the BPR after completion of the batch. To maintain the quality of the product consistently. To follow the effectiveness of corrective action / preventive action To help in the Audit preparation To identify the causes for the quality problems. To follow the GMP records and maintained within the department. To follow line clearance in presence of Q.A person to avoid product and batch mix up. Online filling of batch document for batch packing & Transfer ticket clearance. Filling Temperature and RH control Record To maintain the online documentation as per GMP guidelines. Check on-line entries and that HALB / FERT PO’s are closed. To Prepare the Indents of machine change parts and miscellaneous items through SAP. To maintain quality & quantity of products as per EHS & safety guidelines. Preparation of Protocols equipment’s qualification along with QA and Engg. team and its execution report for any new equipment as and when required To provide feedback for the market compliant for any shortages and quality issue. To take corrective and preventive actions to reduce the market complaints. To check proper packing for the quality and quantity of the products on line

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