Production and Packing planning, Monitoring and reporting daily Production Activities, Master Creation In Pharma Cloud, SAP. IPQA, Document Issuance & Control, CSV, Stability, Validation
EM, Media 111 visual inspection , Aseptic area monitoring, Water and Bioburden testing & Sterility testing & BET Testiug
, IQ, OQ, PQ of equipment, Biological reactivity test - Moda exposure
Evaluates new market complaints daily and communicates them to the various manufacturing partners, determines the criticality of complaints and makes appropriate recommendations. Escalates critical complaints and those with the potential to affect an entire batch or multiple batches.
Should be able to develop analytical methods and perform analysis on UV, Dissolution, HPLC and ICP-OES instruments. Dissolution development, Comparative dissolution profile and multimedia dissolution study.
Person should be well experienced in Environment Monitoring of Injcetable facility Settle plate, air sampling, surface monitoring and personnel gown monitoring. He must be aware of good documentation practices and aseptic behavior.
GPAT is a national level examination for award of scholarship to qualified candidates seeking entry into Master of Pharmacy (M. Pharm) course. The first GPAT was conducted in the year 2010 and thereafter it is conducted every year till 2018 by All India Council for Technical Education (AICTE) as per the directions of Ministry of Education, Government of India and from the year 2019, the examination is conducted through the National Testing Agency (NTA) as per the directions of Ministry of Education, Government of India to till 2023.