? Hybrid | Pharmaceutical Industry Are you passionate about Computer System Validation (CSV) and ensuring compliance in regulated environments? We are looking for a Validation Manager to lead validation activities for a strategic Holistic Data Management (HDM) initiative within a integral pharmaceutical environment. ?

What You'll Do
As Validation Manager, you will be responsible for ensuring that the system meets all applicable validation and compliance requirements throughout its lifecycle.

Key responsibilities
include:
• Own and coordinate all validation activities for the system.
• Prepare, review, and maintain validation documentation, including Validation Plans, Test Documentation, Traceability Matrices, Validation Summary Reports, and related records.
• Lead qualification activities across QA and Production environments, ensuring release readiness.
• Coordinate validation testing activities, deviation management, and defect resolution.
• Ensure compliance with CSV, GxP, GLP, and applicable validation standards.
• Review and support SOPs, AAPs, training materials, and operational documentation required for go-live.
• Collaborate with Business stakeholders, IT System Leads, Quality Assurance, CSV & Compliance teams, and System Owners to support validation approvals and compliance-related activities.
• Act as a key compliance partner during audits, inspections, and system lifecycle activities. ✅ Must-Have Requirements




• Bachelor's degree in Information Technology, Healthcare, Life Sciences, or a related field.
• Strong knowledge of Computer System Validation (CSV) principles and methodologies.
• Expert understanding of regulatory frameworks and guidance, including:
• FDA 21 CFR Part 11
• EU GMP Annex 11
• GxP requirements and validation best practices
• Experience preparing and maintaining validation documentation in regulated environments.
• Solid understanding of validated IT systems, including software, infrastructure, and system integrations.
• Strong analytical, documentation, and stakeholder management skills. ⭐ Nice to Have
• More than 3 years of experience in Computer System Validation within the pharmaceutical, biotechnology, or life sciences industry.
• Experience supporting complex data management, digital transformation, or enterprise applications.
• Previous exposure to audit and inspection readiness activities.
• Experience working within global, cross-functional teams. SCHEDULE ?:
• 08h-17h from Monday to Friday (flexible)
• Full remote CONDITIONS ?:
• Salary package based on

your profile
.
• Permanent contract
• Flexible compensation plan (free of income tax) where we provide you with medical insurance, public transport ticket and childcare check.
• Discounts in gym network.
• Training catalogue.
• Referral program Our goal is that you are well in every way

📌 Validation Manager for Holistic Data Management Project | 100% remote | Pharma (San Cugat del Vallés)
🏢 Ambit Iberia
📍 San Cugat del Vallés