A seasoned expert in pharmaceutical quality, compliance, and supply chain integrity, this speaker brings over 15+ years of hands on experience in the global pharmaceutical and life sciences industry. With a strong foundation in GMP, GDP, and regulatory compliance, currently leads operations at a European pharmaceutical firm specializing in the sourcing, qualification, and distribution of active pharmaceutical ingredients (APIs). Certified in Six Sigma and ISO quality systems, has a proven track record of implementing effective quality management frameworks, managing inspections, and driving audit readiness across complex global supply chains.

A recognized industry trainer and consultant also has contributed to numerous cross-border initiatives involving serialization, cold chain management, and data integrity solutions. Their work bridges regulatory expectations with operational realities, offering practical strategies for safeguarding product quality from manufacturing through distribution. With a deep commitment to continuous improvement and is a respected voice in industry forums and brings a unique blend of technical rigor, regulatory insight, and leadership to every engagement.

The Pop in Your Job: What excites me most about my work is the challenge of navigating complex compliance landscapes and transforming regulatory requirements into efficient, workable quality systems. I enjoy identifying gaps, streamlining processes, and ensuring that every part of the operation aligns with global GMP and GDP standards. There’s a unique satisfaction in leading audits, solving quality issues, and fostering a mindset where compliance is viewed as a value-add, not just a regulatory obligation. I’m driven by the opportunity to influence systems and cultures where quality is built in from the start, and continuous improvement becomes part of daily operations. It’s this ability to blend structure, strategy, and real-world execution that makes my role so rewarding.