Analista Sênior de Farmacovigilância

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.

At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.

We believe that diversity is the driving force behind innovation, creativity, and overall business success.

Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your Role: Pharmacovigilance Associate

As Pharmacovigilance Associate, you will support regional pharmacovigilance operations by managing adverse event and product complaint reporting, supporting customer-focused case handling, and helping maintain compliance with local and global requirements.

In this role, you will work cross-functionally with quality, regulatory affairs, product safety, marketing, and technical teams to support safety reporting, inspection readiness, and continuous improvement across the Latin America region.

Your Responsibilities:


* Report adverse events and product complaints in the global pharmacovigilance database, ensuring compliance with pharmacovigilance procedures and reporting timelines.


* Respond to pharmacovigilance and quality inquiries, support customer-related complaint and refund evaluations, and assist with administrative activities for the Latin America call center.


* Support regional pharmacovigilance compliance activities, including local legal requirements, quality management system requirements, audit and inspection readiness, and follow-up of findings.


* Collaborate with global pharmacovigilance, quality, product safety, data management, marketing, and technical teams on safety monitoring reports, post-marketing study reviews, third-party pharmacovigilance agreement support, and new product launches.


* Contribute to team communications and continuous improvement of regulatory affairs and pharmacovigilance processes across regional affiliates.

What You Need to Succeed (minimum qualifications):


* Degree in life sciences such as Veterinary Medicine, Toxicology, Pharmacy, Chemistry, or equivalent.


* Proven experience in pharmacovigilance within veterinary medicine or the pharmaceutical industry.


* Experience reporting adverse events and product complaints in a pharmacovigilance database in line with required procedures and timelines.


* Proficiency in pharmacovigilance databases and Microsoft Office Suite.

What will give you a competitive edge (preferred qualifications):


* Portuguese and English language proficiency; Spa...