QA Training Specialist | Madrid (Hybrid)Work Schedule : Full-time (40 hours / week), 3 days on-siteAre you detail-oriented, tech-savvy, and passionate about training in a regulated environment? We’re looking for a QA Training Specialist to support a global Gx P training program within a leading life sciences organization.This is a fantastic opportunity to join a growing international team based in Madrid, contributing to global compliance and training excellence across the drug substance network.What You’ll DoAs a QA Training Specialist, you’ll be embedded within the Compliance team and responsible for : Administering and maintaining training records in Success Factors LMS and Veeva DMSSupporting c GMP personnel qualification processes and ensuring documentation accuracyCollaborating with subject matter experts to assign curricula and assess training impactManaging training documentation in line with Gx P regulations and internal SOPsSupporting audit readiness and regulatory complianceInterfacing with platforms like Power BI, Tableau, Smartsheet, and Service NowWhat We’re Looking ForBachelor’s degree with 3–4 years of relevant experience, or Master’s degree with 1–2 yearsHands-on experience with Veeva and Learning Management Systems (LMS) is essentialFamiliarity with GMP environments is a plusStrong organizational and communication skillsAbility to work cross-functionally in a fast-paced, global settingWhy This Role?Be part of a pioneering team advancing cutting-edge medical technologiesWork in a collaborative, international environmentContribute to global health initiatives and regulatory excellenceHybrid working model with a modern office in MadridInterview process : To be confirmed.Interested in making an impact in global training and compliance? Apply now and help shape the future of quality in life sciences.
Quality Assurance Specialist • Madrid, Madrid, SPAIN