Head of QPPV and Office

EU QPPV - remote in Europe.

This full time role will be most suited to talent leaders who already hold a QPPV or Deputy position for a large and global portfolio in pharmaceuticals. You will need to lead on all critical safety/pharmacovigilance issues from the regulatory authorities across all EU markets.

Responsible for:

• Regulatory Compliance
• Safety Surveillance
• Quality Management
• Risk Management
• Reporting
• Team Collaboration

Qualifications:

• Degree in Medicine
• Experience working as a QPPV or Deputy
• In-depth knowledge of EU pharmacovigilance regulations and guidelines.
• Strong understanding of safety surveillance, risk management, and quality management systems.
• Excellent communication, multi-tasking and leadership skills.
• Ability to work collaboratively in a dynamic, fast-paced environment.

If this role is well suited to you then please be in contact to dominic.pritchard@biotalent.com / +41415625046