Experteer Overview In this role you support global pharmacovigilance activities for a broad portfolio of products, ensuring patient safety and regulatory compliance.
You will collaborate with cross-functional teams to manage post-marketing safety surveillance and contribute to safety reporting.
The position offers international exposure and the chance to influence global safety practices.
You join a collaborative environment that emphasizes professional growth and meaningful impact on patients and healthcare professionals.
Compensaciones / Beneficios • Perform routine global pharmacovigilance activities: aggregate reporting, signal detection, literature monitoring, and risk management • Lead and coordinate preparation and review of aggregate safety reports for quality, accuracy, and regulatory compliance • Provide scientific oversight of external pharmacovigilance service providers • Support regulatory submissions, maintenance of marketing authorisations,
and responses to health authority requests • Contribute as SME to upgrades/improvements of PV databases and tools • Prepare and maintain departmental quality documents and support process improvements Responsabilidades • Five+ years of experience in life sciences with significant pharmacovigilance and post-marketing safety exposure at global or HQ level • Strong knowledge of post-marketing PV regulations for medicinal products and awareness of cosmetics regulations • Extensive experience in aggregate reporting, risk management, and signal detection • Experience collaborating with external providers, local affiliates, and cross-functional stakeholders • Strong analytical skills, attention to detail, and ability to manage multiple activities and deadlines • Excellent written and spoken English Requisitos principales • international and collaborative working environment • opportunities for professional development • contribution to general pharmacovigilance activities • meaningful impact on patient safety