The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in ATMP, Biotech, Medical Devices, In Vitro Diagnostics, Digital Health and Pharma.

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QbD has affiliates in 8 different countries and can count on the expertise of more than 500 life science professionals and growing.
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
- Review and approve promotional and non-promotional materials for medicinal products, medical devices in accordance with applicable national and EU regulations, industry codes, and company procedures.
- Provide regulatory advice regarding advertising, promotional claims, scientific communications, educational materials, and patient-facing content.
- Assess compliance of marketing and communication materials before external use.
- Collaborate closely with Medical Affairs, Marketing, Legal, Quality, and Regulatory Affairs teams.
- Support the preparation, maintenance, and lifecycle management of marketing authorizations.
- Contribute to regulatory submissions, variations, renew

📌 Consultant Regulatory Affairs (Madrid)
🏢 Qbd Group | Spain
📍 Madrid