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 doingReview 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 & ExperienceUniversity 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 QualificationsKnowledge 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’reresilientand tackle challenges with a positive mindsetYou’recuriousand always up for learning something newYou have ano non-sense approachhonest, clear, respectfulYou’reinnovativeand bring ideas, not just opinionsAnd above all, you’reserious 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 inJPEG :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)
🏢 NNIT
📍 Madrid