Join Rephine: Leading Life Sciences Quality WorldwideAt Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, India and China, we support the Pharmaceutical, Biotech and Medical Device supply chains globally.Who We're Looking For:Are you a pharmaceutical or analytical laboratory professional with GMP experience looking to take your career into CSV consulting? Do you have hands‑on experience operating laboratory equipment and working under quality standards in a regulated environment? If you are ready to grow into computerised system validation in a integral consultancy that invests in its people, we want you as our next GMP Lab Analyst & CSV Consultant (L3) .Your Role:As an L3 CSV Consultant, you will contribute to validation projects in GxP‑regulated environments, applying your pharmaceutical laboratory knowledge to support the validation of computerised systems used in lab and manufacturing settings.
You will work alongside experienced consultants who will guide your development while you build your CSV expertise.Key Responsibilities:Contribute to the validation of computerised systems used in pharmaceutical laboratory environments (LIMS, ELN, laboratory instruments, analytical software)Prepare and review validation documentation including VMPs, URS, IQ/OQ/PQ protocols, traceability matrices and validation reportsApply your GMP laboratory knowledge to understand system requirements and ensure they meet regulatory standardsSupport deviation management, change controls and CAPA activitiesCollaborate with client laboratory teams, QA and IT to gather requirements and deliver validation activities on scheduleParticipate in client meetings and on‑site laboratory visits as part of project deliveryActively develop your knowledge of GAMP 5, EU GMP Annex 11, FDA 21 CFR Part 11 and Data Integrity guidelines.What We're Looking For:Minimum 1 year of hands‑on experience working in a pharmaceutical,