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Syspro Automation is seeking a CSV Engineer to join a dynamic team tackling exciting automation projects in a GMP environment. Responsibilities include risk analysis, validation documentation, and ensuring compliance, making this a crucial role in the pharmaceutical industry. The successful candidate will have strong experience in CSV, excellent communication skills, and the ability to work autonomously in a fast-paced setting.
In Syspro Automation we are looking for CSV (Computerized System Validation) Engineers to join a multidisciplinary team working in challenging automation projects within a GMP environment.
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Required skills and experience :
Skills that would be a plus :
We offer :