Senior Validation Engineer________________________________________CAI Overview:Are You Prepared to Make an Impact?Established in 1996, CAI is a leading professional services organization that has expanded year after year, now boasting a global workforce of nearly 700 professionals. We specialize in delivering critical solutions within the Life Sciences and Mission Critical sectors, providing comprehensive services including commissioning, qualification, validation, project management, and consulting to ensure operational readiness in FDA-regulated and other high-stakes environments.Our mission is straightforward yet powerful: we strive to be the trusted partner for our clients, assisting them in crafting a better working world and enhancing the human experience.At CAI, we are dedicated to upholding our Foundational Principles both in our professional and personal lives:• Integrity is our core value• We support one another• We contribute to our community• We invest in our futureWe are relentless in our pursuit of excellence, constantly pushing the envelope and exceeding expectations. From our inception, we've dared to challenge the status quo, not only setting industry standards but redefining them entirely. Our innovative mindset and creative methodologies allow us to thrive at the intersection of wisdom, technology, and humanity. For us, operational readiness is not just an objective; it is a way of life. We believe in proactive engagement, meticulous execution, and a commitment to continuous improvement.________________________________________Job Title: Senior Validation EngineerDepartment: Commissioning, Qualification & ValidationReports To: Senior Validation ManagerJob Type: Full-TimeLocation: Dublin, Ireland________________________________________Job Summary:As a Senior Validation Engineer, you will spearhead commissioning, qualification, and validation initiatives for packaging and combination product assembly lines, ensuring adherence to Good Manufacturing Practices (GMP), data integrity, and regulatory compliance. You will collaborate with project teams to formulate and implement validation protocols, oversee documentation processes, coordinate resources, and ensure timely execution of CQV activities. Your early involvement in projects will provide essential design insights, facilitate vendor coordination, and address potential risks, all while partnering with cross-functional teams to achieve optimal outcomes.________________________________________Key Responsibilities:Lead and manage end-to-end validation processes in a GMP environment.
Nov 10, 2025