Join Rephine: Leading Life Sciences Quality Worldwide At 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 general 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 reports

Apply your GMP laboratory knowledge to understand system requirements and ensure they meet regulatory standards

Support deviation management, change controls and CAPA activities

Collaborate with client laboratory teams, QA and IT to gather requirements and deliver validation activities on schedule

Participate in client meetings and on‑site laboratory visits as part of project delivery

Actively 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, biotech or analytical laboratory under GMP or GxP standards

— you have operated laboratory equipment, followed regulated protocols and understand how a compliant lab works

Experience with laboratory instruments such as HPLC, spectrophotometers, balances, autoclaves or similar analytical equipment

Familiarity with laboratory systems such as LIMS, ELN or laboratory software — as a user or administrator

A degree in Pharmacy, Biotechnology, Chemistry, Biomedical Engineering or a related Life Sciences field

Strong attention to detail and documentation skills developed in a regulated environment

Fluency in Spanish and English — both written and spoken

Valid driver’s license and willingness to travel to client sites when required

Genuine interest in computerised system validation and digital transformation in pharma

Why This Role Could Excite You:

Transition from the GMP laboratory into one of the most in‑demand technical profiles in Life Sciences — CSV consulting

Learn from a CSV Director with 25 years of experience and a team of experts who will invest in your growth

Work across multiple pharma clients and laboratory environments — building expertise faster than you would in a single company

Grow towards L2 and beyond with a clear, structured career path

Why Choose Rephine?

Competitive salary aligned to your experience, with annual bonus linked to company objectives

Hybrid model if based in Barcelona / Remote for EU‑based profiles

Occasional travel to client sites and Barcelona office

Birthday gift card and Summer Relax flexibility

2 team building events per year

International project exposure across Spain, UK and Europe

Structured onboarding with dedicated internal trainers

A team where people stay — 10, 20 and even 30 years

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📌 GMP Lab Analyst | CSV Consultant (Barcelona)
🏢 Rephine
📍 Barcelona