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Job Description

Title:Executive

Date: Sep 20, 2025
Location: Guwahati - Operations OSD
Company: Sun Pharma Laboratories Ltd

Monitor and maintain documentation related to QMS activities, including SOPs, change controls, deviations, and CAPAs


Handle market complaints by conducting root cause analysis and implementing corrective actions.


Ensure implementation and compliance with Quality Management System (QMS) guidelines.


Facilitate training programs for personnel on QMS procedures, regulatory requirements, and best practices.


Ensure compliance with Good Manufacturing Practices (GMP) and company policies.


Obtain line clearance as per BMR/BPR, SOP, and checklist.


Follow and execute the daily plan efficiently.


Coordinate with QA, QC, Engineering, and Stores to achieve daily productivity targets.


Conduct the entire packing activity as per written procedures and cGMP guidelines on the shop floor.


Monitor and record in-process parameters online.


Handle the request, receipt, usage, and destruction of stereos.


Maintain work discipline within the department.


Optimize manpower utilization to increase production efficiency per person.


Perform necessary system entries in SAP HANA.


Participate in Technical Training Programs and share knowledge with team members.


Identify safety-related observations and ensure online compliance.


Oversee equipment cleaning, preventive maintenance, and maintain relevant documentation.


Implement measures to improve production yield.


Minimize resource wastage to enhance efficiency.


Reduce changeover time and optimize utilization of both manpower and machinery.


Handle the Track Wise system for OSD packing.


Prepare SOPs via the EDMS system.


Conduct and manage LMS training sessions.


Oversee SAP system operations in OSD packing.


Handle and maintain all types of documentation, related to OSD packing.

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