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Mr. McCullough is a seasoned pharmaceutical and biotech professional with over 25 years of experience in start-up, commissioning, and validation. He has successfully led numerous large-scale projects, ensuring compliance with regulatory standards. His expertise spans quality systems, equipment qualification, and validation planning, with a focus on practical and sustainable solutions. Mr. McCullough has a proven track record of successfully navigating FDA and EU inspections, demonstrating his deep understanding of industry requirements.

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