Global Product Quality Manager – Medical Devices

Galderma S.A.

Barcelona

On-site

EUR 90,000 - 120,000

Full time

14 days+

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Job summary

Galderma is seeking a Product Quality Manager for Medical Devices in Barcelona to lead quality oversight across the product lifecycle, from development to post‑launch. You will influence quality strategy globally, ensuring regulatory alignment and readiness across multiple products and partners.

You will drive inspection readiness, manage risk assessments, CAPAs, and support governance with robust documentation and cross‑functional collaboration.

Qualifications

  • Advanced degree in Life Sciences or related field with regulatory knowledge.
  • Strong understanding of quality systems and lifecycle management.
  • Experience with external partner oversight and regulatory reviews.
  • Familiarity with MDR, GMP, ISO13485 and related standards.

Responsibilities

  • Drive quality oversight for products across development and lifecycle management.
  • Contribute to product development, transfers, validation, and post‑approval changes.
  • Review quality docs, especially Design Control, transfer protocols, reports and risks.
  • Oversee external sites, labs, and partners; support regulatory/CMC reviews.
  • Ensure inspection readiness with proper documentation and traceability.
  • Lead quality risk assessments, CAPAs, and issue resolution.
  • Deliver on assigned tasks; support continuous improvement within quality systems.
  • Provide input, lead activities, and assist governance decision documentation.

Skills

cGMP knowledge
EU MDR knowledge
ISO13485 knowledge
Quality management
Lean Six Sigma
Partner oversight

Education

Advanced degree in Life Sciences

Job description

Galderma is seeking a Product Quality Manager for Medical Devices in Barcelona to lead quality oversight across the product lifecycle, from development to post‑launch. You will influence quality strategy globally, ensuring regulatory alignment and readiness across multiple products and partners.

You will drive inspection readiness, manage risk assessments, CAPAs, and support governance with robust documentation and cross‑functional collaboration.

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