Global Quality Compliance & Audit Readiness Lead - EMEAC

Galderma Services Spain, S.L.; Barcelona; Híbrido; EUR 90.000 - 130.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Diversity & inclusion

Hybrid work culture

Bonus and benefits

Descripción de la vacante

Galderma Services Spain, S.L. in Barcelona seeks a senior audit leader to drive global inspection readiness and manage regional audits across EMEAC.

You will establish frameworks, govern audit programs, and guide cross-regional teams to ensure regulatory preparedness and effective audit outcomes. With at least 10 years in pharma/medical devices audits and fluent English, you will shape strategy, develop capabilities, and advocate best practices across the organization while partnering with

Formación

• Minimum 10 years of audit management experience in Pharma/Medical Devices.
• Fluent English; additional languages are a plus.

Responsabilidades

• Lead and coordinate regionally managed Quality audits (internal, external, and supplier) across EMEAC, ensuring risk-based planning, execution, and timely closure.
• Establish and govern a sustainable global inspection readiness framework to ensure continuous preparedness for regulatory inspections.
• Build, maintain, and enhance auditing capabilities and competencies within regions.
• Proactively monitor regulatory trends and inspection outcomes to strengthen compliance posture and audit effectiveness.
• Develops and maintains the global inspection readiness playbook, including governance model, mock inspections, and sprint readiness.
• Lead end-to-end execution of internal, supplier, distributor, and third-party audits for EMEAC.

Conocimientos

Audit management

Regulatory compliance

English fluency

Descripción del empleo

Galderma Services Spain, S.L. in Barcelona seeks a senior audit leader to drive global inspection readiness and manage regional audits across EMEAC.

You will establish frameworks, govern audit programs, and guide cross-regional teams to ensure regulatory preparedness and effective audit outcomes. With at least 10 years in pharma/medical devices audits and fluent English, you will shape strategy, develop capabilities, and advocate best practices across the organization while partnering with