Full-Time Spain
Oversees all manufacturing and testing activities; ensures cGxP compliance, including data integrity and eCompliance
~ Participates in deviation investigations
~ Reviews and approves records related to manufacturing, quality control, and AS&T (Analytical Science & Technology)
~ Analyzes financial and operational performance
~ Participates in OpEx reduction projects
Qualified Person (QP) – authorizes batch release in accordance with registration data
~ Reports technical complaints, adverse events, or special case scenarios related to Novartis products within 24 hours of receipt
~ Manages the distribution of marketing samples (if applicable)
Key Performance Indicators
~ Manages quality-related aspects and projects within the area of responsibility.
~QC/QA in the pharmaceutical/biotechnology industry, including environmental and cleanroom monitoring
~Extensive functionality
~Cross-organizational collaboration