Analista sr de farmacovigilância – São Paulo/SP [híbrido]

Efetivo (CLT)

Responsabilidades

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.

QUALIFICAÇÕES MÍNIMAS
- 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.
QUALIFICAÇÕES PREFERENCIAIS
- Portuguese and English language proficiency; Spanish is desirable.
- Experience supporting pharmacovigilance compliance in a regional or global environment.
- Experience supporting audits, inspections, or corrective action follow-up within a regulated setting.
- Experience collaborating across quality, regulatory affairs, marketing, technical, and product safety teams.
- Experience supporting product launches or process improvement initiatives in animal health or pharmaceuticals.