Computer System Validation Consultant

Join Rephine – CSV Consultant (L2) – Life Sciences (Remote, based in UK)

At Rephine , we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, we support Pharmaceutical, Biotech, and Medical Device supply chains globally.

We are looking for a Consultant (L2) – CSV to join our team remotely from the UK. This role is ideal for professionals with experience in validation and CSV projects who want to provide senior‑level support to pharmaceutical clients, acting as a trusted consultant and technical reference.

Role Purpose

Provide senior‑level support to pharmaceutical clients in CSV, validation , and potentially other GMP‑related projects, ensuring compliance and delivering high‑quality consultancy services.

Key Responsibilities

• Lead and execute CSV and validation activities (planning, risk assessments, IQ / OQ / PQ, reporting).
• Ensure compliance with GMP, GxP, and Data Integrity requirements.
• Act as the main client contact for validation topics.
• Review and approve validation documentation.
• Provide guidance and mentoring to junior consultants.
• Collaborate with client stakeholders in a consultancy environment.
• Manage project timelines and deliverables to meet client expectations.

Experience & Background

Soft Skills

What You Bring

Why This Role is for You

Why Choose Rephine

For over 20 years , Rephine has helped leading Life Sciences companies improve manufacturing quality processes. Join us to grow your career and make an impact in a fast‑evolving, global company .

Applications must be in English.

Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function

Consulting, Quality Assurance, and Other

Industries

Pharmaceutical Manufacturing

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