PV Associate Analytics & Reporting

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 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.

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 PV Associate – Analytics & Reporting

At Galderma, we’re unique and we embrace difference. As the leading dermatology company in the world, we offer a broad portfolio of products across Aesthetics, Consumer Care and Prescription Medicine. Join us to make a direct impact and help shape the future of dermatology.

We are looking for a Global PV Associate – Analytics & Reporting to support pharmacovigilance activities for our global portfolio of marketed medicinal and cosmetic products, ensuring patient safety, regulatory compliance and effective post-marketing safety surveillance.

Key Responsibilities

• Perform routine global pharmacovigilance activities, including aggregate reporting, signal detection and management, literature monitoring, and risk management.
• Lead and coordinate the preparation and review of aggregate safety reports, ensuring scientific quality, accuracy and compliance with applicable regulations and timelines.
• Provide scientific oversight of external pharmacovigilance service providers.
• Support regulatory submissions, marketing authorisation maintenance and responses to requests from health authorities.
• Contribute as a subject matter expert to upgrades and improvements of pharmacovigilance databases and tools.
• Prepare and maintain departmental quality documents, support process improvements and contribute to operational excellence.

Ideal Profile

• Degree in Pharmacy or another relevant scientific discipline, with at least five years of experience in life sciences.
• Significant experience in pharmacovigilance, particularly post-marketing safety activities at a global or headquarters level.
• Strong knowledge of post-marketing pharmacovigilance regulations for medicinal products, with an understanding of relevant cosmetics regulations and industry best practices.
• Extensive experience in aggregate reporting, risk management methodologies and signal detection for medicinal products.
• Experience collaborating with external service providers, local affiliates and cross-functional stakeholders.
• Strong analytical skills, attention to detail and the ability to manage multiple activities and deadlines.
• Excellent written and spoken English.

What We Offer in Return

• The opportunity to contribute to global pharmacovigilance activities within a leading dermatology company.
• An international and collaborative working environment.
• Opportunities to develop your expertise and contribute to continuous improvement and operational excellence.
• The chance to make a meaningful impact on product safety and patient well-being.

Next Steps

Our recruitment process typically includes an initial conversation with Talent Acquisition, an interview with the Hiring Manager and further discussions with relevant stakeholders.

Our people make a difference. Join Galderma and help us advance dermatology for every skin story.