EU Licensed QPPV
Job Summary
Working remotely on a full-time basis, the EU Licensed QPPV will manage the establishment and maintenance of pharmacovigilance systems, ensure compliance with regulatory requests, and oversee the safety aspects of medicinal products.
Key responsibilities
- Establish and maintain a system for collecting and collating information on suspected adverse reactions
- Respond promptly to requests from Competent Authorities for additional information regarding medicinal product evaluations
- Oversee safety profiles and emerging safety concerns related to the company's medicinal products
Required qualifications
- Life-science education background in Medicine (human or veterinary) or Pharmacy preferred
- Solid knowledge of pharmacovigilance system operations and functions
- Strong understanding of global regulations and best practices in safety processing and reporting
- Proven experience in a pharmacovigilance role, with significant experience as a QPPV
- Strong oral and written English communication skills
Complete Job Description
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