← Toutes les offres

Ambit Iberia fournit des services technologiques et de conseil aux entreprises, notamment dans les sciences de la vie.

Repères sur Ambit Iberia
Domaine officiel
ambit-iberia.com
Offres ouvertes
13

Détails de l’offre

La description complète publiée par Ambit Iberia.

Voir l’offre originale ↗

Description de l’offre

At Ambit, we are looking for an experienced Senior Validation Manager to join a strategic initiative within a leading global pharmaceutical company. The successful candidate will play a key role in the validation of the Medicine Data Foundation (MDF) , a next-generation data platform designed to enable data-driven decision-making across the Medicine domain. The first major use case supported by MDF will be the Risk-Based Quality Management (RBQM) initiative, making this a unique opportunity to contribute to the validation of modern data products in a highly regulated environment.

This role is ideal for professionals with extensive experience in Computer System Validation (CSV) , strong knowledge of GxP regulations , and a background in validating complex data, analytics, or cloud-based platforms within the pharmaceutical industry.

Key Responsibilities

  • Define and lead the validation strategy for the Medicine Data Foundation (MDF).
  • Develop and maintain Validation Plans, Validation Assessments, Validation Reports, and associated validation documentation.
  • Apply risk-based validation methodologies aligned with GxP requirements and industry best practices.
  • Assess platform capabilities, controls, data flows, and validation scope/boundaries.
  • Ensure end-to-end traceability between business requirements, system functionality, risk assessments, testing activities, and validation evidence.
  • Support the validation needs of the RBQM initiative as the first strategic consumer of MDF data products.
  • Collaborate closely with Quality, IT, Data & Analytics teams, Product Owners, Solution Architects, and Business stakeholders.
  • Manage validation-related risks, deviations, CAPAs, and inspection readiness activities.
  • Provide expert guidance on CSV, Data Integrity, and regulatory compliance.
  • Contribute to the creation of reusable validation frameworks, standards, and assets for future data platforms and data products.

Required Qualifications

Must-Have:

  • 10+ years of experience in Computer System Validation (CSV) within the pharmaceutical, biotechnology, or regulated healthcare industry.
  • Strong knowledge of GxP regulations , validation methodologies, and compliance requirements.
  • Proven experience defining validation strategies for complex enterprise systems or platforms.
  • Extensive experience leading validation activities throughout the full system lifecycle.
  • Strong stakeholder management, communication, and leadership skills.
  • Fluent English (written and spoken). Nice-to-Have:
  • Experience validating Data Platforms, Data Lakes, Data Warehouses, or Analytics solutions.
  • Knowledge of Microsoft Azure, Microsoft Fabric, or other modern cloud-based architectures.
  • Familiarity with Data Products, Data Mesh, and enterprise data platform concepts.
  • Experience supporting Clinical Development, Medicine, Quality, Regulatory Affairs, or R&D data initiatives.
  • Exposure to Risk-Based Quality Management (RBQM), Central Monitoring, Clinical Data Analytics, or related disciplines.
  • Experience with Veeva or other Life Sciences digital platforms. What We Are Looking For We are seeking a senior consultant who combines:
  • Deep expertise in CSV and GxP validation.
  • Strong understanding of modern data and analytics ecosystems.
  • Experience within the pharmaceutical or life sciences industry.
  • Strategic mindset with the ability to define scalable validation approaches.
  • Excellent communication and stakeholder engagement capabilities. Expected Deliverables
  • Medicine Data Foundation Validation Strategy.
  • Validation Plan and Risk Assessment.
  • Traceability Framework.
  • Validation Execution Oversight.
  • Audit and Inspection Readiness
  • Support.
  • Reusable Validation Assets for future Data Products.
  • Validation
  • Support for RBQM implementation. SCHEDULE 🕘:
  • 08h-17h from Monday to Friday (flexible)
  • Hybrid CONDITIONS 🌱:
  • Salary package based on your profile.
  • Permanent contract
  • Ticket restaurant included in-office hours.
  • 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. Our goal is that you are well in every way!

Candidater à cette offre

Comment candidater ?

L’offre est publiée sur le site de Ambit Iberia. Ouvrez l’offre originale ↗ pour y déposer votre candidature. Screeningpass ne remplit pas de formulaire à votre place.

À qui écrire chez Ambit Iberia pour ce poste ?

Lancez une recherche de contact depuis cette page. Screeningpass vous propose jusqu’à trois personnes liées au poste. Vous choisissez celle à qui écrire, puis Screeningpass cherche son e-mail professionnel et prépare un message. Vous le relisez et l’envoyez vous-même avec Gmail. Une adresse e-mail n’est pas toujours disponible, et une réponse n’est jamais garantie.

Combien coûte la recherche d’un contact ?

Une recherche coûte 1 crédit. Le crédit vous est rendu si la recherche échoue. L’inscription offre 3 crédits, soit 3 recherches.

À quoi sert Screeningpass ?

Screeningpass rassemble des offres de stage, d’alternance et d’emploi publiées par les entreprises. Pour une offre, Screeningpass trouve une personne à contacter dans l’entreprise, cherche son e-mail professionnel et prépare un message à partir de votre CV. Voir le fonctionnement en détail.