- 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
- Solid analytical and problem-solving skills.
- Ability to work as part of team.
- Experience in Automation and Test Management tool
Call me (phone hidden) or mail :
[email protected]
📌 LS GXP Validation testing (Hyderabad)
🏢 Acesoft Labs
📍 Hyderabad