Title: Executive - QMS

Date: Oct 6, 2025

Location: Jammu - Operations

Company: Sun Pharma Laboratories Ltd

To raise and get approval of UPD / PD / Change control and get approval from authorities.
Handle LMS related activities and their timely completion.
To do and arrange CFT meeting of related to QMS.
To receive the market complaints and get closer timely after discussion with CFT team.
To review and arrangement of all GMP format requirement like formats / log etc.
Prepare yearly calibration schedule and their completion timely.
To implement and monitor the CAPA.
To complete the schedule training / on job training .
To maintain / follow the cGMP / GQS guideline requirements..
To handle change control, deviation and other GMP compliance related documents and ensure that all compliance related documents get closed within its time frame.
Prepare all types of audit response like internal / external and any other regulatory authorities.
Prepare and arrange new / schedule revision SOP and their archival.
Archival and maintain of all formats.
Maintain SOP index time to time of all packing related SOPs.