EU-QPPV
Compass Human Resources Group A/S
Our client is entering an exciting phase of growth and is centralizing its EU QPPV function in Denmark. This represents a unique opportunity to take on a highly influential role with responsibility for ensuring that the company’s Pharmacovigilance team and framework continues to evolve in line with business growth, regulatory requirements, and international expansion.
Shape the Future of Pharmacovigilance
As EU QPPV, you will serve as the company’s Pharmacovigilance expert and trusted advisor to senior leadership. You will be responsible for maintaining, developing, and strengthening the organisation’s Pharmacovigilance capabilities while ensuring that patient safety remains firmly embedded across the business.
The role combines strategic influence with operational responsibility and offers the opportunity to lead and further develop the Pharmacovigilance function and team in a dynamic and entrepreneurial environment characterised by close collaboration, short decision-making processes, and a strong growth agenda.
Key Responsibilities
As EU QPPV, you will:
• Act as EU QPPV and hold overall responsibility for the Pharmacovigilance system and PSMF
• Ensure regulatory compliance, inspection readiness, and lead interactions with health authorities, auditors, and inspectors
• Oversee safety surveillance activities, including signal management, risk evaluation, and postauthorisation commitments
• Develop and strengthen Pharmacovigilance processes, systems, and governance to support continued growth and international expansion
• Support regulatory submissions, safety variations, licensing activities, and market expansion initiatives
• Manage external Pharmacovigilance vendors and partners
• Lead and develop the Pharmacovigilance team, driving awareness and collaboration across the organisation
Your Profile
We are looking for an experienced Pharmacovigilance professional who is qualified to act as EU QPPV and thrives in an environment where strategic oversight and hands-on execution go hand in hand. You bring extensive experience within EU Pharmacovigilance and a strong understanding of GVP requirements, combined with a proven track record of developing, optimising, and strengthening Pharmacovigilance systems, processes, and governance frameworks. You have successfully managed inspections, audits, health authority interactions, and CAPA processes, and are comfortable operating in a highly regulated environment where compliance and business priorities must be balanced effectively.
About the Company
Our client is a dynamic and rapidly growing pharmaceutical company with a strong presence across several European markets. Through strategic partnerships, licensing activities, and product acquisitions, the company has developed a diversified portfolio spanning branded medicines, generic medicines, and niche specialty pharmaceuticals.
The organisation combines strong regulatory expertise with an entrepreneurial mindset and a collaborative culture built on teamwork, accountability, and integrity. Employees are empowered to take ownership, contribute ideas, and continuously improve the way the business operates, while maintaining a strong focus on patient impact, trust, and long-term growth.
Interested in Learning More?
The recruitment process is carried out in collaboration with the consulting company, Compass Human Resources Group. If you want to learn more about this position before submitting your CV, please do not hesitate to contact Senior Director, Tom Zehngraff at +45 22 66 18 18 or Senior Research Consultant, Rebecca Saks at +45 21 84 95 32. As we process CVs continuously, we encourage you to submit your CV at your earliest convenience if you are interested. Please note that all inquiries will be handled with confidentiality and that we will reply to the email address from which your CV is sent.
Deadline for applications: As soon as possible
Workplace: Copenhagen
Reference: 2601.123
Company: Anonymous
