A seasoned biopharma leader with over 29 years of experience in manufacturing, quality assurance, and regulatory compliance. As Vice President of Manufacturing at Entos Pharmaceuticals, he drives the development of GMP-grade genetic medicines. Colleagues describe him as an excellent team leader, motivating, and a thought leader in the industry.
He is passionate about innovation, operational excellence, and advancing the biopharma sector with patient-centric solutions. He actively shares insights on regulatory reforms, new GMP guidelines, and the adoption of technologies like e-learning and AI to improve workforce skills and compliance within the industry.
He has contributed to key industry guides for the International Society for Pharmaceutical Engineering (ISPE).
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