E821 | Validation Consultant Pharma - Hybrid

Would you like to work in a global, multicultural and multilingual team as a Validation Consultant providing demand management, project management and data integrations serving to connect systems with each other in a multinational pharmaceutical?WHAT WILL BE YOUR MISSIONTake into account business needs as well as regulatory requirements and standards to define the strategy and documentation for validation concepts.Validate some qualification projects like ECM Data Migration and some Decommissioning projects.Environment: Middleware infrastructure systems (SAP Process Orchestration, SAP CPI, Informatica Cloud, etc.
).WHAT WILL MAKE YOU SUCCEED IN THIS POSITIONBachelor's or Master's Degree with a major focus on IT, engineering, sciences, pharmaceuticals, or biotechnology (or an equivalent field).Experience in project implementation using computer validation (CSV) regulations and methods (e.g.
SOPs and Corporate Procedures, GCP, FDA Guidelines, 21 CFR Part 11) and Data Integrity experience.+5 years of experience in GxP/NonGxP.Experience in Agile working methods is a plus.Fluent in written and spoken English.BENEFITSPermanent Contract.Ticket restaurant included if you come to the office in person.Flexible Retribution Program (medical insurance, public transport ticket and childcare check).Discounts on gym network (Wellhub).SCHEDULEFrom Monday to Friday: 08 am to 17 pm / 09 am to 18 pm (flexible).1 day of office work | 4 days by remote.100% remote (OUT of Barcelona).Our goal is that you are well in every way!
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