Senior QA Auditor – Global Audit Team (Pharmaceuticals & Consumer Health)Location:Dublin, Ireland (preferred) or within mainland EuropeWork Model:Hybrid (Office / Home / Travel)Travel Requirement:Approx. 40% annually, mainly within Europe (25 audits per year)OverviewAn international healthcare organisation is expanding itsQuality Assurance (QA) Audit Teamand is seeking aSenior QA Auditorto join a growing, high-performing group. This is a fantastic opportunity for a motivated and autonomous professional looking to advance their QA career while working alongside a collaborative and experienced leadership team.The audit function plays a critical role in upholding the company's reputation, compliance standards, and commercial performance. The team conducts audits across a diverse portfolio includingpharmaceuticals,medical devices,cosmetics, andfood supplements, with a primary focus onGMP-regulated pharmaceutical suppliers.This role will appeal to professionals eager to take ownership of their work, travel across Europe, and gain exposure to a wide range of contract manufacturers, laboratories, material suppliers, warehouses, and logistics providers.Scope of the RoleThe Senior QA Auditor will:Plan, coordinate, lead, or participate in GMP and supplier auditsManage the end-to-end audit lifecycle, from scoping to CAPA closureDraft and communicate audit scopes and agendas (when acting as lead auditor)Prepare for and execute audits efficiently and independentlyAnalyse audit findings and identify compliance issues or systemic gapsReport findings and ensure follow-up on CAPAs to verify effective closureContribute to continuous improvement initiatives within the audit programRepresent the company's values while engaging with external partnersThis position requires a proactive professional with excellent attention to detail, strong time management, and the ability to prioritise independently while working collaboratively within a team environment.Required Experience & Qualifications5+ years' experience in Quality Assurance within the pharmaceutical industry, ideally including external supplier auditingSolid knowledge of GMP and EU/US regulatory frameworksIRCA certification or equivalent auditing qualification (preferred)Third-level degree in Chemistry, Biology, Pharmacy, Engineering, or a related fieldStrong analytical, communication, and reporting skillsProficiency in Microsoft Office and familiarity with quality systems (e.g., TrackWise)Willingness and ability to travel frequently within EuropeBenefits & Work EnvironmentCompetitive compensation and benefitsHybrid working (typically 2 days remote per week when not travelling)Strong focus on employee development, career progression, and work-life balanceSupportive and values-driven team culture