Ben Green

Before joining the PMO team at Broughton in 2019, Ben held a number of senior QC and supply chain positions within the Pharmaceutical industry, working on pandemic response & global vaccine campaign launches.

  • Ben has over 10 years experience in a number of key roles within FDA & MHRA regulated industries, including development and testing of pandemic vaccines and delivery systems in use globally, Manufacturing and supply chain process management, as well as quality auditing & engagement with FDA & MHRA inspectors.
  • He has coordinated a significant number of regulatory submissions to both the FDA’s CBER and CTP offices, most recently developing and leading successful delivery of PMTA submissions for major clients in the next generation nicotine industry.

Ben holds a BSc (Hons) in Applied Biomedical Science and began his career in vaccine research and diagnostics, supporting vaccine development, production and rapid pandemic response as part of the quality control microbiology department. Moving into operations & supply chain, gave him the opportunity to plan, manage & deliver global vaccine campaigns.

Ben has delivered several major and complex projects for key clients, showing a keen passion for regulatory compliance & development of strategies to best place clients in a position to successfully meet the application & marketing requirements of the FDA and MHRA.

In his ability to develop excellent professional relationships, Ben has a proven track record of working alongside clients in identifying opportunities to bring new products to market & utilize efficient processes for delivery of regulatory submissions on time & in-budget.

Ben is committed to ensuring clients are able to access the very latest regulatory intelligence in consultation with Broughton to successfully bring their life-enhancing products into the commercial space.