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.Main responsibilities :Conduct risk analysis and define validation plans for various process equipments in the pharmaceutical industry.Review documentation of the equipments to ensure compliance with the validation plan.Define, execute and document qualification tests.Manage and document deviations and changes.Required skills and experience :Minimum of 5 years of experience in CSV validation.Strong skills in managing and creating documentation (Microsoft Word and Excel).Excellent communication skills and proactive attitude.Ability to work independently and as part of a team.Experience within the biotech industry with knowledge of current Good Manufacturing Procedures (cGMP).English level B2 or better.Skills that would be a plus :Experience with DeltaV systems is a strong plus.Knowledge of Kneat documentary platform is a plus.We offer : Permanent contract.Remote or hybrid work options in our offices in Nigrán, Madrid and Lisbon.Integration into a young and highly skilled team.Opportunities for professional development and continuous training.
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