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Ergomed
Qualified Person Responsible For Pharmacovigilance (QPPV) In The EU And UK
Remote · Spain · Full time · Senior level
About the role
The EU QPPV ensures safety information collection, regulatory communication, and oversight of medicinal product safety within the EU and UK. The role requires continuous availability to authorities and managing safety profiles and compliance.
What you’ll do
• Establish and maintain adverse reaction information system. • Respond promptly to regulatory authority requests. • Provide relevant safety information to authorities. • Be continuously available to authorities and ensure backup. • Oversee safety aspects of medicinal products.
What you’ll bring
• Life-science education in Medicine or Pharmacy preferred. • Solid knowledge of pharmacovigilance system operations. • Strong knowledge of global safety regulations and compliance. • Proven operational and managerial skills. • Extensive experience as QPPV with strong English communication.
Life at Ergomed
Offers training and career development, supportive environment, and global collaboration. Values diversity, equity, inclusion, and work-life balance.
About Ergomed
PrimeVigilance, part of Ergomed PLC, is a global pharmacovigilance service provider supporting pharmaceutical and biotech partners with medical information, regulatory affairs, and quality assurance.