The process was highly professional and intellectually stimulating. It consisted of two intensive rounds involving local and global management (Australia). The interviewers dived deep into my pharmaceutical background, specifically my experience in QC and GMP environments. It wasn't just a simple Q&A; it was a rigorous assessment of how I bridge the gap between laboratory workflows and IT solutions. We discussed complex scenarios regarding LIMS implementation, data integrity (ALCOA+), and technical troubleshooting involving SQL and API integrations.
