Close up portrait of Andrew Willis

Andrew Willis

SVP, Regulatory, CMC & Quality

Andrew has more than 35 years of experience with Pharmaceutical Development, Regulatory Affairs and Quality Assurance. Experience at multiple senior levels within pharmaceutical companies, gaining significant experience in coordinating, planning and running global development projects from a Quality, CMC and Regulatory perspective. Andrew has worked in major CDMOs and CROs including Cardinal Health, Catalent and Theorem and Pharmaceutical Companies, including Pfizer and has been involved in developing multiple product types, providing oversight and direction on products as diverse as ATMPs, cancer vaccines and biosimilars.