CSV CONSULTANT

Are you an experienced Computer System Validation (CSV) Consultant looking for your next challenge in the Life Sciences sector? I’m working on behalf of a global consulting firm with over 20 years of experience delivering top-tier quality assurance and GxP compliance solutions to leading Pharmaceutical, Biotech, and Medical Device companies worldwide. With offices in Barcelona, the UK, and China, this organisation is known for driving innovation and excellence across the industry.They are now seeking a CSV Consultant to join their team in Barcelona. This is a fantastic opportunity for a professional eager to make a meaningful impact on compliance projects across Spain, Europe, and beyond.What You’ll Be Doing:As a CSV Consultant, you will:Lead validation projects for computerised systems, covering all stages of the project lifecycle, from drafting documentation like VMPs to conducting IQ, OQ, and PQ testing.Ensure compliance with industry regulations, including EU GMP Annex 11, FDA 21 CFR Part 11, GAMP 5, and Data Integrity guidelines.Work with cutting-edge systems like ERPs, eDMS, eQMS, LIMS, SCADA, EBR, and pharmacovigilance platforms, assessing their compliance and readiness.Conduct audits of software suppliers and provide compliance risk assessments with actionable solutions.Collaborate directly with clients, delivering high-impact results while adhering to agreed timelines and standards.What We’re Looking For:To succeed in this role, you’ll need:A Bachelor’s degree in Chemistry, Engineering, or a related field.Proven experience in the pharmaceutical or life sciences industry, particularly in GxP compliance and computerised system validation.Strong multitasking and project management skills, with the ability to balance client needs across multiple projects.Fluency in Spanish and English is essential.A valid driving licence and willingness to travel to client sites (often not accessible by public transport).Why This Opportunity?This position offers:Competitive Compensation: A salary that reflects your experience, plus additional holiday entitlement and other benefits.Flexibility: Hybrid working options, flexible hours, and shorter Fridays.Global Exposure: Opportunities to collaborate with a multicultural team and work on international projects.Professional Growth: A supportive environment where your career can thrive, with opportunities to develop your skills and take on leadership roles.Dynamic Work Environment: Join a motivated, enthusiastic team working on cutting-edge projects in Life Sciences.Is This You?Do you enjoy working closely with clients to solve critical challenges? Can you confidently navigate complex regulatory requirements while maintaining strong communication and collaboration? If you’re passionate about advancing quality and compliance in the Life Sciences industry, this could be the perfect next step in your career.If this opportunity resonates with you, I’d love to discuss it further. Please reach out to me directly to explore whether this role is the right fit for your experience and career goals.