Join our Enterprise Technology & Performance team as a seasoned Computer System Validation (CSV) Consultant. You will drive functional excellence and innovation by ensuring the integrity and compliance of enterprise applications within the life sciences and healthcare sectors.

This role offers a dynamic environment where your expertise in quality assurance and system validation is crucial for supporting global business operations and long-term growth.

Lead end-to-end validation activities for enterprise applications, including ERP, LIMS, QMS, and MRP systems. Develop and implement validation strategies to ensure agility and speed in delivery.

Create and review critical validation deliverables such as Validation Plans, URS, FRS, and test reports. Manage deviations, conduct root cause analysis, and implement CAPA. Support supplier assessments and provide guidance on regulatory compliance.

We seek an experienced professional with at least 5 years in quality assurance or computerized system validation within the regulated life sciences and healthcare industry. A strong understanding of GxP, 21 CFR Part 11, and EU Annex 11 is essential.

Key skills include hands-on experience with enterprise-level applications, data migration, cloud validation, and risk assessments. Excellent communication and interpersonal skills are vital for collaborating with stakeholders across all organizational levels.