Kymos Group is seeking a Quality Assurance Scientist for its GLP area in the QA Department. The role focuses on reviewing and auditing analytical documentation, supporting self-inspections, and ensuring GLP/GCP compliance in all processes.
The adecuado candidate holds a degree in chemistry, pharmacy, or biosciences with at least 1 year of QA or clinical/preclinical trial experience in the pharmaceutical industry.
Strong
English and Spanish are required.
📌 GLP QA Scientist — Hybrid, Flexible Hours & Growth (Madrid)
🏢 Kymos Group
📍 Madrid
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