Title: Executive
6 days ago
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 closure 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.
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