Intas is one of the leading multinational pharmaceutical formulation development, manufacturing, and marketing organization in the world. It has been growing at 19% CAGR and crossed the $2.5 billion mark in the past financial year. The company has set up a network of subsidiaries, under the name Accord Healthcare in the EU, US, Canada, SA, Australia, APAC as well as CIS & MENA regions. Intas is present in 85+ countries, with more than 70% of its revenue coming from global business..
Greetings from Intas Pharmaceutical Limited..!!!!
Important Details :
API:
· To perform Computer system validation
· To investigate deviation, change request, OOS, market complaint etc.
· To review & closer of Deviation, Change Control, CAPA, out of specification, investigation
· To prepare & review of Quality risk assessments report
· To prepare process validation protocols & reports, cleaning validation protocols & reports.
· To perform QC instrument qualification & Calibration
· To review analytical data, raw data if method validation and method transfer
· To review & closre of OOC, OOT etc with proper investigation
· To control the record & monitor of all the activities for stability chamber & retain sample
· Digital Initiatives, Training, Regulator support & APQR
· DMF updation as and when required by regulatory department
· Global CAPA review & closure
To perform IPQA activity
· QA digitisation
Documentation (Librarian) & QA Release
Join Intas Talent Network. Mail your CVs to hrd_valia@intaspharma.com
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