Descrição da Função
Your new company
Join an international pharmaceutical company assuming the Pharmacovigilance & Regulatory Affairs Specialist position, based in Lisbon.
Your new role
This professional will be responsible, in Pharmacovigilance area, for processing Individual Case Safety Report, submitting this in a global database, updating medicines in XEVMPD, and preparing SOPs. Will additionally be responsible for training staff and KPI monitoring. In Regulatory Affairs area, this professional will prepare dossiers for medicines, medical devices and food supplements, manage the lifecycle of the products and review packaging material.
What you'll need to succeed
We are looking for a professional with at least 3 years of experience in Pharmacovigilance area, in Pharmaceutical Industry and a Degree in Life Sciences. Fluency in English is mandatory. This person should be proactive, team player, and organized.
What you'll get in return
This is an excellent opportunity to join a growing international company, who values their human resources.
What you need to know
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
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