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Hash was previously Director of Technical Development at Mundipharma and was responsible for leading the Chemistry, Manufacturing and Controls (CMC) of global assets. He has expertise covering the full development of Drug Substance, for both complex protein and small molecules, and their Drug Products including, parenteral administration, oral-solid and medical devices for inhalation. Hash has many years of experience in the strategic and operational management of global contract development and manufacturing organisations (CDMOs) and has successfully advanced assets from discovery to First-in-Human studies and then from clinical research to commercialisation. Earlier in his career, he held senior programme management positions at CDMOs including Lonza Biologics and later served with several small biotechs, culminating in a partnership at Pulmagen Therapeutics LLP.