Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else. At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. We have established a Global Capability Center in Barcelona to support Galderma's growth trajectory and our global commercial and functional teams. Located in the upscale Eixample district in the heart of the city, it offers the possibility for professional career development through exposure to global and cross‑functional projects.

Global Pharmacovigilance Risk Minimization Physician – Therapeutic Dermatology Location: Barcelona, SpainAt Galderma, we're unique and we embrace difference. Whether it’s the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products, or our commitment to recognising and rewarding people for the contribution they make – working here isn’t like anywhere else. At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Summary

As part of the continued evolution of our Global Pharmacovigilance organization, we are looking for a Global Pharmacovigilance Risk Minimization Physician to join our Therapeutic Dermatology (TD) team in Barcelona.



This role will be responsible for leading key post‑marketing safety activities for Galderma's approved TD products, with a primary focus on Nemluvio (nemolizumab) but also including additional TD products. The position will play a critical role in ensuring continuous benefit‑risk assessment, maintaining regulatory compliance, and supporting the safe use of our innovative therapeutic dermatology treatments worldwide. The successful candidate will combine strong medical expertise, pharmacovigilance knowledge, and global stakeholder management skills to provide scientific leadership throughout the product lifecycle.

Key Responsibilities

Post‑Marketing Safety and Risk Management

- Lead ongoing benefit‑risk assessments for assigned TD Galderma products, ensuring appropriate identification, evaluation, and management of safety risks.
- Provide medical expertise for post‑marketing safety activities, with primary responsibility for Nemluvio and support for additional TD products.
- Lead signal detection, validation, evaluation, and escalation activities using safety data, including individual case safety reports and aggregate safety information.
- Develop and maintain Risk Management Plans (RMPs) and support implementation of risk minimization strategies across global markets.
- Provide medical input into safety analyses,



aggregate reports, and relevant safety documentation throughout the product lifecycle.

Regulatory Compliance and Inspection Readiness

- Ensure compliance with global pharmacovigilance regulations and internal safety standards.
- Support preparation for regulatory authority inspections and act as a subject matter expert during audits and inspections.
- Maintain inspection readiness by ensuring appropriate oversight of PV processes, controlled documentation, SOPs, and work instructions.
- Support the development and implementation of Corrective and Preventive Actions (CAPAs) following inspections or quality assessments.
- Contribute to maintaining a robust Pharmacovigilance Quality Management System (QMS).

Scientific Leadership and Cross‑Functional Collaboration

- Act as a medical and scientific partner across functions including Clinical Development, Medical Affairs, Regulatory Affairs, Quality, Commercial, and other global stakeholders.
- Represent Global Pharmacovigilance in relevant governance forums, safety committees, and cross‑functional working groups.
- Communicate complex scientific and safety concepts clearly to both technical and non‑technical audiences.
- Provide scientific guidance and confidently challenge stakeholders when required to ensure patient safety and regulatory compliance.
- Build effective relationships with internal teams and external partners across general markets, including collaboration with international business partners.

Continuous Improvement and Operational Excellence

- Identify opportunities to improve pharmacovigilance processes, increase efficiency, and strengthen ways of working.

📌 Global Pharmacovigilance Risk Minimization Physician (Barcelona)
🏢 Galderma Services Spain
📍 Barcelona