QA Training Specialist | Madrid (Hybrid)
Work Schedule : Full-time (40 hours / week), 3 days on-site
Are 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 GxP 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 Do
As a QA Training Specialist, you’ll be embedded within the Compliance team and responsible for :
- Administering and maintaining training records in SuccessFactors LMS and Veeva DMS
- Supporting cGMP personnel qualification processes and ensuring documentation accuracy
- Collaborating with subject matter experts to assign curricula and assess training impact
- Managing training documentation in line with GxP regulations and internal SOPs
- Supporting audit readiness and regulatory compliance
- Interfacing with platforms like PowerBI, Tableau, Smartsheet, and ServiceNow
What We’re Looking For
Bachelor’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.