Equipment Validation Specialist
Job Overview:
The Equipment Validation Specialist will be responsible for ensuring the qualification and maintenance of pharmaceutical equipment, utilities, and systems in a validated state.
Main Responsibilities:
1. Develop, execute, and review Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols for sterile manufacturing equipment.
2. Maintain the validated state of manufacturing equipment, clean utilities, and process support systems.
3. Qualify and validate aseptic filling lines, lyophilizers, autoclaves, depyrogenation tunnels, and isolator/RABS systems.
4. Support clean utilities qualification (e.g., WFI, clean steam, compressed air, HVAC).
Key Requirements: A Bachelor’s or Master’s degree in Engineering or Life Sciences; At least 5 years of experience in validation, equipment qualification, or technical services within sterile injectables manufacturing.