Global QC Lead: Inspection Readiness & EMEAC Audits

Galderma

Barcelona

Hybrid

EUR 110,000 - 170,000

Full time

5 days ago
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Benefits offered by this job

Bonus structure
Extended benefit package
Hybrid work culture

Job summary

Galderma is seeking a Global Quality Compliance Inspection Readiness & EMEAC Audits Manager to lead and coordinate regionally managed quality audits across EMEAC, ensuring risk-based planning, execution, and timely closure. You will establish a sustainable global inspection readiness framework and build auditing capabilities within regions.

You will monitor regulatory trends, drive readiness sprints and mock inspections, and ensure traceability of findings and corrective actions across the

Qualifications

  • Minimum 10 years of experience in a role focused on audit management in a Pharma/Medical Devices environment.
  • Broad types of audits performed covering the regulated areas pertaining to Galderma's portfolio (cosmetics, medical devices, pharmaceuticals)
  • Fluent English (additional languages are a plus)

Responsibilities

  • Lead and coordinate regionally managed Quality audits (internal, external, and supplier) across EMEAC.
  • Establish and govern a sustainable global inspection readiness framework for regulatory inspections.
  • Build, maintain, and enhance auditing capabilities within regions.
  • Proactively monitor regulatory trends and inspection outcomes to strengthen compliance posture.
  • Lead end-to-end execution of internal, supplier, distributor, and third-party audits for EMEAC.

Skills

Audit management
Quality compliance
Regulatory knowledge
Leadership
Cross-regional collaboration

Job description

Galderma is seeking a Global Quality Compliance Inspection Readiness & EMEAC Audits Manager to lead and coordinate regionally managed quality audits across EMEAC, ensuring risk-based planning, execution, and timely closure. You will establish a sustainable global inspection readiness framework and build auditing capabilities within regions.

You will monitor regulatory trends, drive readiness sprints and mock inspections, and ensure traceability of findings and corrective actions across the

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