Hyderabad
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Key Responsibilities
- Execute and monitor validation activities for sterile injectable manufacturing processes.
- Prepare, review, and maintain validation protocols and reports.
- Perform qualification activities including:
- DQ, IQ, OQ, and PQ for equipment and utilities
- HVAC validation
- Water system validation
- Compressed air and nitrogen validation
- Coordinate process validation and media fill activities.
- Perform cleaning validation and hold time studies.
- Ensure compliance with cGMP, SOPs, and regulatory guidelines.
- Review validation documentation and ensure proper data integrity practices.
- Coordinate with Production, Engineering, QC, and Microbiology departments.
- Handle deviations, change controls, CAPA, and risk assessments related to validation.
- Support internal audits and regulatory inspections.
- Maintain validation master plans and schedules.
- Location Hyderabad
- Website
[email protected]
- Salary Best in Industry
- EXPERIENCE NEED
📌 QA Executive – Validation (Injectables) (Hyderabad)
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📍 Hyderabad