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 years
Hands-on experience with Veeva and Learning Management Systems (LMS) is essential
Familiarity with GMP environments is a plus
Strong organizational and communication skills
Ability to work cross-functionally in a fast-paced, global setting
Why This Role?
Be part of a pioneering team advancing cutting-edge medical technologies
Work in a collaborative, international environment
Contribute to global health initiatives and regulatory excellence
Hybrid working model with a modern office in Madrid
Interview 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