Description
Responsible 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.
Qualifications
M.Pharmacy or Any Postgraduate.
📌 Sr Executive Qa Kukatpally
🏢 Aveva Drug Delivery Systems
📍 Kukatpally
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