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Ass. Manager QA
Difgen Pharmaceuticals
Hyderābād
Full-Time
0-3 Years experience
Description
| Review of exhibit batch manufacturing records and exhibit batch packing records before execution of the batch. * Responsible for review of process validation protocol and reports, hold time protocol and reports. * Responsible for review of executed media fill records for regulatory submissions. * Responsible for review and submission of executed exhibit batch manufacturing records and batch packing records. * Responsible for review and submission of process validation reports and hold time reports. * Responsible for review and submission of intended batch manufacturing records. * Responsible for review and submission of product related equipment's qualification documents. * Responsible for review of QMS documents like Change control, deviation and CAPA. |
About Difgen Pharmaceuticals
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