Consultant Regulatory Affairs

No deje pasar esta posibilidad, inscríbase rápidamente si su experiencia y habilidades coinciden con lo que se indica en la siguiente descripción.

Location: Hybrid - Madrid
Type: Full-time

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

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