ppWhether 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. /ppGlobal 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. /ph3Summary /h3pAs 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. /ph3Key Responsibilities /h3h3Post‑Marketing Safety and Risk Management /h3ulliLead ongoing benefit‑risk assessments for assigned TD Galderma products, ensuring appropriate identification, evaluation, and management of safety risks. /liliProvide medical expertise for post‑marketing safety activities,



with primary responsibility for Nemluvio and support for additional TD products. /liliLead signal detection, validation, evaluation, and escalation activities using safety data, including individual case safety reports and aggregate safety information. /liliDevelop and maintain Risk Management Plans (RMPs) and support implementation of risk minimization strategies across global markets. /liliProvide medical input into safety analyses, aggregate reports, and relevant safety documentation throughout the product lifecycle. /li /ulh3Regulatory Compliance and Inspection Readiness /h3ulliEnsure compliance with global pharmacovigilance regulations and internal safety standards. /liliSupport preparation for regulatory authority inspections and act as a subject matter expert during audits and inspections. /liliMaintain inspection readiness by ensuring appropriate oversight of PV processes, controlled documentation, SOPs, and work instructions. /liliSupport the development and implementation of Corrective and Preventive Actions (CAPAs) following inspections or quality assessments. /liliContribute to maintaining a robust Pharmacovigilance Quality Management System (QMS). /li /ulh3Scientific Leadership and Cross‑Functional Collaboration /h3ulliAct as a medical and scientific partner across functions including Clinical Development, Medical Affairs, Regulatory Affairs, Quality, Commercial, and other integral stakeholders. /liliRepresent Global Pharmacovigilance in relevant governance forums, safety committees, and cross‑functional working groups. /liliCommunicate complex scientific and safety concepts clearly to both technical and non‑technical audiences. /liliProvide scientific guidance and confidently challenge stakeholders when required to ensure patient safety and regulatory compliance. /liliBuild effective relationships with internal teams and external partners across global markets, including collaboration with international business partners. /li /ulh3Continuous Improvement and Operational Excellence /h3ulliIdentify opportunities to improve pharmacovigilance processes, increase efficiency, and strengthen ways of working. /liliSupport initiatives related to automation, process optimization, and reduction of operational complexity.



/liliPromote a proactive safety culture focused on continuous improvement and patient protection. /li /ulh3Skills and Qualifications /h3ulliMedical Degree (MD or equivalent) required. /liliMinimum 10 years of experience within the pharmaceutical industry, with significant experience in global positions within Global Pharmacovigilance and post‑marketing safety. /liliStrong expertise in: Signal detection and safety surveillance. /liliRisk management activities. /liliBenefit‑risk assessment. /liliGlobal pharmacovigilance regulations and compliance requirements. /liliExperience working with biologics and understanding of their safety monitoring requirements. /liliDemonstrated experience supporting regulatory inspections, inspection readiness activities, Quality Management Systems (QMS), and CAPA management. /liliProven experience working in a global environment, collaborating across regions. /liliExperience with dermatology, immunology, and other specialty therapeutic areas is highly desirable. /liliStrong communication, influencing, negotiation, and stakeholder management skills, with the ability to confidently challenge and align with senior colleagues. /liliAbility to work independently, manage complexity, and operate effectively in a changing and dynamic environment. /liliProactive, agile, and solution‑oriented mindset with strong ethical standards and professional integrity. /liliFluent English communication skills required. /li /ulh3What we offer in return /h3ulliWe offer a hybrid working model. /liliWe offer professional development opportunities. /liliThe opportunity to grow within a leading global dermatology organization. /li /ulh3Our people make a difference /h3pAt Galderma, you’ll work with people who are like you – and people who are different. We value what every member of our team brings. Professionalism, collaboration, scientific curiosity, and a supportive ethos create the perfect environment for people to thrive and make a real impact. /ppGalderma is the emerging pure‑play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science‑based portfolio of premium flagship brands and services that span the full spectrum of the fast‑growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin we are in shapes our lives, we are advancing dermatology for every skin story. /ppFor more information go to /p /p #J-18808-Ljbffr

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