EU QPPV

BioTalent is partnered with a leading Pharmaceuticals to appoint a EU QPPV who is based in Spain. This full time role will be most suited to those who already hold a QPPV or Deputy position and can lead on critical safety/pharmacovigilance issues from the regulatory authorities.

Responsible for:

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

Qualifications:

• Degree in Pharmacy, Medicine, or related field.
• Experience working as a QPPV or in a senior pharmacovigilance role in the pharmaceutical industry.
• In-depth knowledge of Spanish and EU pharmacovigilance regulations and guidelines.
• Strong understanding of safety surveillance, risk management, and quality management systems.
• Excellent communication 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