Overview We are looking for a Validation Technician who will offer service to a pharmaceutical company. Managing Validation Documentation, in charge of multiple validation projects and their agendas.SkillsUniversity studies with postgraduate or Master\'s degree (Chemical Engineering, Industrial Engineering, Biotechnology).Knowledge and practice of office automation at an advanced level: Microsoft Office.Desirable: 3-5 years or more experience in a similar position, preferable validating SAPKnowledge and experience in/with:Spanish and/or English (Minimum B2)Pharmaceutical Sector (GxP)21 CFR Part 11 and EU GAMP Annex 11 regulationsGAMP 5Computerized Systems Validations (CSV)English (Minimum B2)Good Communication SkillsTasksDefinition of validation strategies.Generation of validation documentation (Validation Plan, Risk Analysis, Qualification Protocols: IQ, OQ, PQ, reports).Support and help to the staff that will be functionally in charge of it, for the revision of documentation.Management of the schedule of different projects under your responsibility for validations.Communication with the work team (project status, incidents detected, etc.).Schedule08/09h -17/18h from Monday to Friday (flexible)Possibility of 100% remote working (Willingness and readiness to travel occasionally like the onboarding)ConditionsSalary package based on your profile. We will discuss it on our first call.Permanent ContractFlexible Retribution Program (medical insurance, public transport ticket and childcare check)Discounts on gym network(Andjoy)Learning & DevelopmentFriend Referral ProgramOur goal is that you are well in every way!#J-18808-Ljbffr