SVU Technova is looking for a Pharma Validation Executive with hands-on experience in equipment qualification and validation across Sterile, Formulation, and API manufacturing facilities.

The candidate will be responsible for executing the complete validation lifecycle from URS to PQ, along with computerized system validation (CSV) documentation and regulatory compliance.

Key Responsibilities

- Preparation and execution of URS, DQ, FAT, SAT, IQ, OQ & PQ.
- Validation of Sterilization Equipment – Autoclaves, FBD, Sterilizers, Depyrogenation systems, etc.
- Validation of Formulation Equipment – Manufacturing vessels, FBD, Co-mill, Octagonal Blender, Compression, Coating, etc.
- Validation of API Equipment – Reactors, Centrifuges, Dryers, Filters, Vacuum systems,



etc.
- Preparation of risk assessments, validation protocols, test scripts and reports.
- Equipment functional and performance verification.
- Preparation and review of CSV documentation for PLC/SCADA/HMI and computerized systems.
- Knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5 and Data Integrity.
- Support deviation, change control, CAPA and validation lifecycle management.
- Coordinate with clients, OEMs and engineering teams during validation activities.
- Prepare audit-ready validation documentation.

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📌 Pharma Validation Executive (Hyderabad)
🏢 SVU TECHNOVA
📍 Hyderabad