🔍 Drug Safety Trainee (Vet Profile)

📍 Location: Hybrid
🕓 Type: Full-time

QbD Group team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in Pharmacovigilance.

💡 What’s in it for you?

Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices

Grow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.

Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.

A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.

🏢 What you’ll be doing

• Comply with the timetable and respect its rules of operation, safety and occupational risk prevention.
• Comply with the training project following the instructions of the tutors (both QbD's internal training and the training provided by the clients in the projects involved).
• Case management (data entry, control of pharmacovigilance cases in post-marketing and/or clinical trials, or related to medicinal, health and cosmetic products).
• Contact with HCP and patients/consumers (for follow-up information).
• Handling medical information and responding to any complaints.
• Support in local and international literature search activities.
• Support in authority search activities.
• Support in website/social media monitoring.
• Support in reconciliation activities.
• Support in any other type of departmental activity.
• Teamwork, both with people from the PV department and with colleagues from MI, Regulatory Affairs and Clinical Trials.

💪 What you bring

Studies required:

• University degree in Veterinary Medicine.
• Postgraduate degree related to the pharmaceutical industry. Desirable.

Required skills:

• High spoken and written level of English. Must.
• Ability to work in a team and social and communication skills. Must.
• Analytical and detail-oriented skills. Desirable.
• Knowledge of MS Office desirable. Desirable.
• Demonstrable interest in the pharmaceutical industry and pharmacovigilance.

🫵 Who you are

Our culture is driven by values If this sounds like you, you’ll fit right in:

• You’re resilient and tackle challenges with a positive mindset
• You’re curious and always up for learning something new
• You have a no non-sense approach honest, clear, respectful
• You’re innovative and bring ideas, not just opinions
• And above all, you’re serious about your work, but not too serious about yourself

✨ About us

We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.

We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.

You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.

📩 Interested? Let’s talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.