# Validation Manager for Holistic Data Management Project \| 100% remote \| Pharma at Ambit Iberia > Remote · Spain · Manager · Other · open. Source: https://alderhq.app/jobs/teamtailor%3Aambit%3A7be5c65e-7c4d-4d62-96f5-231d4cff826a (read 2026-11-09). ## Facts (observed) - Company: [Ambit Iberia](https://alderhq.app/companies/ambit-iberia) - Location text: Sant Cugat del Vallès, Spain - Where it can be done from (inferred): Remote · Spain (evidence: "Remote role open worldwide") - Posted: 2026-11-05 (4 days ago) - First seen by alder: 2026-11-07 · last verified: 2026-11-07 - Reposted: 0 times · edited: 0 times - Apply on the employer's site: https://ambit.teamtailor.com/jobs/8673271-validation-manager-for-holistic-data-management-project-100-remote-pharma ## Pay and sponsorship - Posted pay: not posted - Market band for similar posted roles (Spain, n 42): p25 €51k, median €67k, p75 €88k ## Description (the employer's text) 📍 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 global 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! --- Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/teamtailor%3Aambit%3A7be5c65e-7c4d-4d62-96f5-231d4cff826a and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.