I'm currently partnering with a global, industry‐leading pharmaceutical company that is expanding its manufacturing operations and looking for multiple levels of experience in CSV & Data Integrity professional to support key initiatives across a diverse range of manufacturing systems.
This role involves driving Computer System Validation and Data Integrity activities, ensuring compliance with international regulatory standards, and collaborating closely with process owners, engineering teams, and quality functions. It offers the opportunity to make a significant technical impact within a major biopharmaceutical environment.
Ideal candidates will bring:
* Experience in Computer System Validation and Data Integrity within a GMP pharmaceutical manufacturing setting
* Strong familiarity with DeltaV, PI, PCS7, PLC, SCADA, and alarm management practices
* Solid understanding of FDA, EMA, and global regulatory requirements, including hands‐on experience with risk‐based validation
* Strong project coordination, documentation, and change management capabilities
* Excellent communication skills with fluency in English (additional languages are a plus)
If you're interested in exploring this exciting opportunity with a global pharmaceutical leader, I'd be happy to share more details -please apply or reach out for a confidential discussion!