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0.0 years

0 Lacs

jammu, jammu & kashmir, india

On-site

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 do...

Posted 1 week ago

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