Global Pharmacovigilance Risk Minimization Physician – Therapeutic Dermatology Applylocations: Full timeposted on: Posted Todayjob requisition id: JR Galderma 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 , 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. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world.

Further supporting our growth and innovation momentum, we are establishing a new Global Capability Center in Barcelona to deploy new capabilities to effectively support its global commercial and functional teams. Located in the upscale Eixample District in the heart of Barcelona, Galderma's Global Capability Center offers numerous possibilities for professional development such as exposure to global and cross-functional projects and access to global career opportunities. Global Pharmacovigilance Risk Minimization Physician – Therapeutic DermatologyLocation: At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. SummaryAs 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.

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. 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.

Build effective relationships with internal teams and external partners across global markets, including collaboration with international business partners. Support initiatives related to automation, process optimization, and reduction of operational complexity.

Minimum 10 years of experience within the pharmaceutical industry, with significant experience in global positions within Global Pharmacovigilance and post-marketing safety.

Global pharmacovigilance regulations and compliance requirements.

Experience working with biologics and understanding of their safety monitoring requirements.

Demonstrated experience supporting regulatory inspections, inspection readiness activities, Quality Management Systems (QMS), and CAPA management.

Proven experience working in a global environment, collaborating across regions.

Experience with dermatology, immunology, or other specialty therapeutic areas is highly desirable.

Strong communication, influencing, negotiation, and stakeholder management skills, with the ability to confidently challenge and align with senior colleagues.

Proactive, agile, and solution-oriented mindset with strong ethical standards and professional integrity.

Fluent English communication skills required. What we offer in returnAt Galderma, you will have the opportunity to contribute to the safety strategy of innovative dermatology treatments and make a meaningful impact on patients worldwide. You will work in a collaborative global environment where scientific excellence, innovation, and patient safety are at the heart of everything we do.

We offer a hybrid working model, professional development opportunities, and the opportunity to grow within a leading global dermatology organization. Next StepsIf your application is successful and your profile is a match, you will be invited for:

A first virtual conversation with the recruiter.

A virtual interview with the Hiring Manager.

- Additional interviews with key stakeholders from the Integral Pharmacovigilance organization. #

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