Leading Life Sciences Quality WorldwideAt Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. Aumente sus posibilidades de conseguir una entrevista leyendo la siguiente descripción general de este puesto antes de presentar su candidatura. With offices in Barcelona, the UK, India and China, we support the Pharmaceutical, Biotech, and Medical Device supply chains globally.Who We're Looking ForAre you passionate about building your career in CSV consulting within the Pharma and Life Sciences sector?

If you're excited by the challenge of validating computerised systems in a general consultancy with the highest quality standards, we want you as our next CSV Consultant (L3) in Barcelona.Your RoleAs an L3 CSV Consultant, you will be an active contributor to validation projects, working alongside experienced consultants and under the guidance of senior team members. Key ResponsibilitiesCSV Project ExecutionContribute to the validation of computerised systems (ERP, LIMS, eQMS, eDMS, SCADA, laboratory systems) in GxP-regulated pharmaceutical environments.Ensure compliance with EU GMP Annex 11, FDA 21 CFR Part 11, GAMP 5 and Data Integrity guidelines.Quality & ComplianceSupport deviation management, change controls and CAPA activities.Contribute to supplier audits and compliance assessments under senior supervision.Client & Team CollaborationWork closely with cross-functional client teams (QA, IT, business owners)



to gather requirements and deliver validation activities on schedule.Participate in client meetings and on-site visits as part of project delivery.Collaborate with your project team and Area Manager to ensure quality and timely delivery.Learning & DevelopmentActively develop your knowledge of GxP regulations, validation methodologies and pharma systems.Participate in Rephine's internal training programme and knowledge-sharing sessions.Why This Role Could Excite YouBuild deep CSV expertise across a wide range of systems and pharma clients — in two to three years at Rephine you'll learn what would take five years in a single company.Be part of a growing global consultancy where your contributions are visible and valued from day one.What You BringA Bachelor's degree in Chemistry, Engineering, Pharmacy, Biotechnology or a related Life Sciences field.Some experience in the pharmaceutical industry and GxP-regulated environments — whether in CSV, QA, or a related technical role.Ability to manage your own workload across multiple tasks and projects.Fluency in Spanish and English, with strong written communication skills.Valid driver's license and willingness to travel to client sites when required.Are you ready to commit to a consulting career and everything that comes with it — variety, pace, client interaction and continuous learning?Do you take ownership of your work and hold yourself to a high quality standard?Benefits: Medical insurance, pension plan and flexible salary scheme (Spain), plus birthday gift card and Summer Relax.Hybrid model, flexible hours Monday to Thursday, and intensive Fridays all year round.24 days holiday per year (Spain).Global Exposure: Work with a multicultural team across Spain, UK, Europe and beyond. xsgfvud Career Path: A structured progression from L3 to L2, L1 Tech and Line Director — with real mentorship at every stage.Culture: A team where people stay — 10, 20 and even 30 years — because the environment is worth it.Location: Barcelona — Hybrid ·Apply in English ·

📌 Validation Software Consultant | GxP & Life Sciences (Barcelona)
🏢 Rephine
📍 Barcelona