Senior CSV Validation Lead - Enterprise Platforms (Remote)

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The candidate will lead end‑to‑end validation activities for enterprise‑level software systems and manage teams, stakeholders, and delivery for global programs.

Key Responsibilities • Lead end‑to‑end validation lifecycle (Planning, Risk Assessment, Testing, Release, Periodic Review) • Drive validation strategy for enterprise programs across regions (Europe/Global) • Manage validation teams, allocate work, and ensure timely delivery • Act as primary point of contact for client stakeholders and leadership • Lead governance, status reporting, and escalation management • Author and review validation deliverables (URS, FRS, IQ/OQ/PQ, RTM, Validation Report) • Ensure compliance with 21 CFR Part 11, EU Annex 11, Data Integrity (ALCOA+) • Support regulatory audits and inspection readiness • Mentor and coach junior resources, build capability within the team • Drive continuous improvement and standardization of validation processes Managerial Skills • Team leadership and people management • Stakeholder and client relationship management • Program and project management for global validation initiatives • Risk and issue management with mitigation planning • Resource planning and capacity management • Governance, reporting, and executive communication • Budget awareness and delivery management • Cross‑functional coordination across IT, QA, Business and Vendors • 10+ years of experience in Life Sciences CSV/CSA • Exposure to cloud/SaaS validation • Strong experience in enterprise systems (SAP S/4HANA, Veeva Vault, LIMS, QMS, etc.) • Understanding of SDLC and validation lifecycle • Understanding of regulatory guidelines (GAMP 5, GxP, 21 CFR Part 11, EU Annex 11, etc.) • Experience in risk‑based validation and CSA approach • Experience working with US and European clients and regulated environments • Strong documentation, communication, and leadership skills Role: System Validation, Platform Qualification Location: Spain (100% Remote) | Salary: Market Range | Permanent full‑time position Requirements and number of open positions 3–5 years – 2 positions in open 5–10 years – 2 positions in open 10+ years – 2 positions in open Role Overview We are looking for a highly experienced Validation resource with 10+ years of experience in Computerized System Validation (CSV) within the Life Sciences domain.