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Computer Systems Validation (CSV) Specialist | Pharma (Hybrid)

Ambit Iberia | sant cugat del vallès, Spain | Posted June 05, 2026

Position Overview

We are looking for a Computer Systems Validation (CSV) Specialist to play a key role in ensuring compliance with regulatory requirements and internal standards by leading validation efforts throughout the system lifecycle. This position requires strong collaboration across cross‑functional teams and a solid understanding of risk‑based validation methodologies.

Tasks & Responsibilities

  • Ensure that all validation activities are properly planned and executed in accordance with validation strategies, GxP requirements, and applicable BI SOPs prior to system go‑live.
  • Maintain the system’s validated state throughout its lifecycle.
  • Collaborate closely with Quality Assurance (QA) on compliance‑related topics.
  • Coordinate with System Owners, Process Owners, Business Process Owners, System Leads, Developers and other stakeholders.
  • Ensure that all system‑specific SOPs and System Lifecycle (SLC) documentation are in place before s...

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