QPPV/PV Manager

Frost Pharma

Sweden - Stockholm

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Would you like to be part of a rapidly growing pharmaceutical company dedicated to providing hospital medicines for both children and adults in the Nordic market? In this pivotal position as QPPV/PV Manager, you will take on key responsibilities within Pharmacovigilance, ensuring patient safety and compliance. This is an exciting opportunity to be part of a team that is expanding across the Nordics, working in a dynamic, fast-paced environment focused on innovation and patient benefit.

The position

We’re seeking an experienced professional with solid expertise in Pharmacovigilance and in-depth knowledge of Good Vigilance Practice (GVP). In this crucial role, you’ll lead the company’s PV operations, serve as the QPPV for the FrostPharma´s own products, and manage medical information. While working independently, you’ll closely collaborate with the Quality and Regulatory teams to ensure smooth coordination across departments.

You will have the opportunity to join a growing company during an exciting expansion phase where the learning curve is steep and you will be part of a team dedicated to innovation and enhancing patient care. This is a full-time position located at our headquarters in Danderyd, Stockholm.

Responsibilities:

• Lead Pharmacovigilance and Medical Information.
• PV responsibility for the company’s own products.
• Literature search, handling RMPs and PSURs, signal detection, and risk management materials.
• Reconciliation processes.
• Handle PV inspections and audits.
• Review and sign pharmacovigilance agreements (SDEAs).
• Update Standard Operating Procedures (GVP).
• Conduct GVP trainings (introductory and annual).
• Act as QPPV and maintain the company’s pharmacovigilance system and PSMF.
• Receive, follow up, and document adverse event reports in accordance with local quality systems and agreements with external partners.

Qualifications:

• Pharmacist, natural science, or healthcare background.
• Deep knowledge and experience in GVP.
• At least 5 years of experience in all areas of Pharmacovigilance.
• Experience as QPPV from the pharmaceutical industry.
• Completed ICSR and XEVMPD training and qualified for Eudravigilance database registration.
• Fluent in Swedish and English, both written and spoken.
• Experience in medical information is a plus.

Personal Attributes

We are seeking an individual with strong integrity and a reliable personality who is detail-oriented and responsible. You thrive in independent work, take initiative, and tackle challenges with a pragmatic approach. Your communication skills are effective both internally and externally, and you possess a curious mindset, always eager to grow and develop in your role within an entrepreneurial environment.

Location:
Stockholm, Sweden

Scope: full-time

About FrostPharma
FrostPharma is a rapidly growing Swedish pharmaceutical company dedicated to the commercialization and availability of value-added specialist and hospital medicines. Since signing our first product agreement in 2017, we have developed a portfolio of approximately 50 essential products. This growth has been fueled by our proactive business development efforts, leading to new product rights and the creation of our own offerings.

We have established a strong commercialization platform for specialist medicines across the Nordics and are actively planning to expand into more countries within the EU. Our product portfolio is primarily aimed at hospital settings and includes specialist medicines where treatments are initiated in hospitals.

The next step - your application
If this opportunity has captured your attention and you are truly ready to engage with genuine interest and commitment, we invite you to apply today or contact Kristina Edholm (Senior Recruitment Manager) at PharmaRelations for a confidential conversation. Interviews are being conducted continuously.

Thank you.