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

📋 Description

• Establish and maintain a system that ensures information about all suspected adverse reactions
• Ensure that any request from the Competent Authorities for provision of additional information
• Provide to the Competent Authorities any other information relevant to the evaluation of the
• Be continuously available to Competent Authorities in Member States and the Agency and the MAH
• Have oversight of the safety aspects of the company's medicinal products including an overview of

🎯 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 regarding safety processing
• Strong operational and managerial skills as demonstrated by leading previous projects or functions
• Strong experience in a PV role, 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 based all over the world, with English as the company language