Consultant Medical Information
- German

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) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in ATMP, 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 General

Responsibilities:
Assume the responsibilities of Information Officer, a mandatory role in Germany. Carry out activities specific to the area, including the execution of assigned projects and direct interlocution with clients, ensuring high-quality delivery and client satisfaction. Act as a reliable scientific partner to clients, demonstrating a strong understanding of their needs, therapeutic areas,

Conduct general and local bibliographic searches, European Agency searches,



authority searches and safety literature monitoring in compliance with GVP requirements. Participate in Regulatory Pharmacovigilance Intelligence activities, including monitoring and interpretation of regulatory updates, health authority alerts, safety trends and emerging risks. Specific

Responsibilities:
Perform assigned Quality activities within the area (deviations, CAPAs, change controls), supporting timely resolution and compliance with QMS requirements. Review and adapt QbD Group SOPs and working instructions to ensure alignment with client-specific procedures and regulatory requirements. Contribute to the definition and monitoring of Medical Information metrics and KPIs, supporting performance tracking and continuous improvement. Participate in internal and external MI training activities, including onboarding, continuous development and PSP-related training. Support project coordination for assigned clients across delegated Medical Information, Medical Enquiries, PSP call center and Pharmacovigilance Intelligence activities, collaborating with internal and external resources as required. Create, validate and maintain automated search alerts tailored to each client's product portfolio and therapeutic area. Perform weekly review, documentation and reporting. Perform searches within European Medicines Agency (EMA) databases, including: Application of QbD Group-defined filters (MLM) Download and reconciliation of IC SRs when applicable L2A case downloads Conduct Authority Searches by reviewing Regulatory Agency websites to identify health alerts, safety communications, variations in product information, and other relevant regulatory updates. P

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📌 Consultant Medical Information (Pozuelo De Alarcón)
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📍 Pozuelo de Alarcón