Contract Details
Contract Duration: 3 to 6+ Months (Rolling Contract)
Job Type: Contract (Office-based)
Location: Nivelles, Brussels, Belgium
Work Setup: Onsite
Compensation: Up to 400 EUR/day
Notice Period: Immediate / ASAP
A leading global consultancy is seeking a skilled CSV Analyst for a high-impact pharmaceutical client project in Belgium. This role is critical in managing validation processes across SAP environments, with full lifecycle involvement from planning to audit support.
Responsibilities
* Define and manage validation activities (planning, authoring, testing, traceability) for changes and projects.
* Collaborate with the IT Compliance Lead to define the validation strategy.
* Prepare and facilitate key deliverables including Validation Plans, Test Protocols (IQ/OQ/PQ/MQ), Reports, and Traceability Matrices.
* Coordinate test execution with system owners and business testers.
* Track deviations, lead investigations, and manage related CAPAs.
* Ensure audit readiness and provide support during regulatory inspections.
* Provide updates and participate in weekly status meetings with stakeholders.
* Act as deputy to the IT Compliance Lead when needed.
Requirements
* Bachelor’s/Master’s degree with 3+ years in Computer System Validation (CSV).
* Hands-on experience with SAP Validation (SAP ECC and/or S/4 HANA) and compliance standards like GxP, GMP, GDP, GLP.
* Solid background in writing/leading test protocols (IQ/OQ/PQ/MQ).
* Proven ability to manage compliance documentation and audits.
* Excellent English communication skills; French is a strong plus.
* Familiarity with pharma processes, especially quality management and mobile/web apps.
Capable of working autonomously and managing complex validation timelines.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance
Industries
Software Development
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