Consultant Regulatory AffairsLocation: Hybrid - MadridType: Full-timeThe 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 devicesGrow 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, renewals,



and compliance activities.- Monitor regulatory developments related to pharmaceutical advertising and promotional practices.- Support audits, inspections, and internal compliance initiatives where required.- Maintain documentation and records in accordance with internal quality systems.What you bringQualifications & Experience- University degree in Pharmacy, Life Sciences, Medicine, or a related scientific discipline.- At least 3-5 years of experience in Regulatory Affairs within the pharmaceutical industry.- Proven experience in review and approval of promotional and non-promotional materials.- Strong knowledge of Spanish pharmaceutical advertising requirements and relevant EU legislation.- Experience working in a cross-functional and international environment.- Excellent written and verbal communication skills in Spanish and English.- Strong attention to detail and ability to manage multiple priorities.Preferred Qualifications- Knowledge of medical information, scientific communications, and compliance processes.- Experience supporting multiple pharmaceutical products and therapeutic areas.Who you areOur 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 yourselfAbout usWe 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.#J-18808-Ljbffr

📌 Consultant Regulatory Affairs - Promotional & Non-Promotional Materials (Madrid)
🏢 TRIUM Clinical Consulting
📍 Madrid