Global Quality Compliance Inspection Readiness & EMEAC Audits

Overview

In this role you will lead global quality audits and build a sustainable inspection readiness framework to support regulatory inspections across EMEAC. You will develop and enhance auditing capabilities, monitor regulatory trends, and guide regions to strengthen compliance. The position offers cross-functional exposure within a growing, diverse organization focused on dermatology. You will impact audit governance, readiness, and the company’s regulatory posture.

Pay / Benefits

• hybrid work culture
• competitive compensation with bonus
• extended benefit package
• global career opportunities
• ownership from day one

Responsibilities

• Lead regionally managed quality audits (internal, external, supplier) across EMEAC with risk-based planning and timely closure
• Establish and govern a global inspection readiness framework ensuring preparedness for regulatory inspections
• Develop and continuously enhance auditing capabilities within regions
• Monitor regulatory trends and inspection outcomes to strengthen compliance and audit effectiveness
• Develops and maintains the global inspection readiness playbook, governance model, mock inspections, and readiness sprint methodology
• Design and deploy a structured, risk-based Global Mock inspection program
• Lead inspection readiness sprints prior to anticipated regulatory inspections with remediation prioritization
• Monitor global inspection outcomes and regulatory trends to strengthen defence capability
• Lead end-to-end execution of internal, supplier, distributor, and third-party audits for EMEAC
• Administer the global auditor qualification framework
• Provide guidance and system support to LATAM, US, JPAC regions
• Ensure traceability of audit activities, findings, and corrective actions with timely closure and consistent application of Good Practices
• Escalate critical regulatory compliance issues with global suppliers/vendors and define action plans
• Share audit trends and risk insights across regions to support inspection readiness
• Provide functional direction to regional audit leads regarding inspection readiness standards

Key requirements

• Minimum 10 years of audit management experience in a Pharma/Medical Devices environment
• Broad types of audits across cosmetics, medical devices, and pharmaceuticals
• Fluent English; additional languages a plus

• leadership
• cross-functional collaboration
• proactive problem solving
• audit management across regulated areas
• regulatory inspection readiness
• global auditor qualification framework

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