Panel Discussion
Monday, March 23
05:55 PM - 06:40 PM
Live in Everett
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As advanced technologies reshape pharmaceutical manufacturing, organizations are challenged to evolve their approach to quality assurance. This panel brings together industry leaders to explore how digital transformation is redefining quality culture, risk mitigation, and regulatory compliance. The discussion will focus on how companies can build proactive resilience, leverage data and analytics for continuous improvement, and foster a culture of innovation that supports both compliance and sustainable growth. Panelists will share real-world insights into balancing technological advancement with organizational adaptability in an increasingly complex global landscape. To be discussed:
With over 20 years of experience in IT management, security, operations, and systems design, I am a leader and advisor in the digital domain. As the CIDO/CTO at Polpharma, one of the largest pharmaceutical companies in Europe, I oversee the strategic direction and execution of IT initiatives that support the business goals and enhance the customer experience.
My core competencies include project management, IT auditing, quality systems, information security, and systems architecture. I have a proven track record of implementing and establishing best practices, standards, and frameworks for IT governance, compliance, and performance. I have also led and contributed to multiple projects that involved digital disruption, transformation, and innovation, leveraging my expertise in TOGAF, ISMS, and IT security. I am passionate about creating value and impact through IT solutions that are aligned with the business vision and mission.