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Senior Validation Manager | Hybrid (Pharma)
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.…
Information about Ambit Iberia
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- ambit-iberia.com
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- 13
Job details
The full description published by Ambit Iberia.
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!
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