Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (homebased)

📋 Description

• Establish and maintain a system ensuring collection and collation of all suspected adverse reaction
• Ensure prompt and full responses to requests from competent authorities for additional information
• Provide competent authorities with other information relevant to benefits/risk evaluation
• Be continuously available to competent authorities and the MAH, ensuring adequate back-up procedures
• Oversee safety aspects of the company's medicinal products, including safety profiles, emerging

🎯 Requirements

• Life-science education background; Medicine (human or veterinary) or Pharmacy preferred
• Solid knowledge of PV system operations and function
• Strong knowledge of global regulations, standards, and best practices in safety processing
• Strong operational and managerial skills demonstrated by leading projects or functions
• Strong PV experience, profound experience as QPPV
• Strong oral and written English communication skills

🎁 Benefits

• Training and career development opportunities internally
• Strong emphasis on personal and professional growth
• Friendly, supportive working environment
• Opportunity to work with colleagues worldwide, with English as the company language