Have sound knowledge and experience in CSV in pharma.
Understand FRA, Execute OQ's
Create and maintain validation documents like Operational qualification, Test Reports
Knowledge of Regulations and guidelines like 21 CFR part 11, EU annex 11, GDPR
Robust analytical and problem-solving skills.
Ability to work as part of team.
Experience in Automation and Test Management tool
me or mail:
📌 Ls Gxp Validation Testing Hyderabad (India)
🏢 Acesoft Labs
📍 India
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