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.Syspro Automation is an engineering company focused on GMP Automation, working globally with offices in Spain, Portugal, Switzerland and the United States.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 4 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 C1 or better.Skills that would be a plus:
- Knowledge of Kneat documentary platform is a plus.- Spanish language is also a plus.We offer:
- Permanent contract.- Hybrid work with at least 2 days in our office in Nigrán.- Integration into a young and highly skilled team.- Opportunities for professional development and continuous training.