QPPV

Work from anywhere and make a difference in pharmacovigilance which drives results! Enjoy the freedom of remote work while making a global impact.

R&D Partners is seeking an experienced EEA QPPV to oversee pharmacovigilance activities and ensure compliance with EU and UK regulations. This role involves managing PV systems, supporting regulatory interactions, and acting as the primary contact for competent authorities and inspections.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Serve as the nominated EEA QPPV in line with EU Directive 2001/83/EC and GVP guidelines.
• Maintain oversight of product safety profiles, risk management plans, and signal detection.
• Ensure compliance with PV legislation and quality standards, including PSMF accuracy.
• Act as 24/7 contact point for authorities and lead PV audits.
• Support clients in regulatory meetings and provide PV expertise.

Key Skills and Requirements:

• Life science degree (pharmacy, medicine, biology, chemistry, etc.).
• Minimum 5 years’ pharmaceutical industry experience.
• Strong knowledge of EU PV regulations and GVP.
• Ability to manage PV systems and work cross-functionally.

For more information, please contact William Tyler.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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