PV Associate Analytics & Reporting

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 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.