Ass. Manager QA

## Ass. Manager QA

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| 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. |

## Any PostGraduate

M. Pharmacy or Any Postgraduate.