Director Quality and Regulatory Affairs
B.App.Sc. Analytical Chemistry & Microbiology
Julie has more than 30 years’ experience in the life sciences industry. This includes 20 years’ experience with pharmaceutical manufacturing company, FH Faulding, and 10 years with SeerPharma as a GMP consultant. Whilst working in the industry, Julie held technical and project management roles across research and development, including technology transfer to routine manufacture, as well as management positions within IT. These roles also involved working on clinical trials, and submissions to regulatory authorities.
As a senior GMP consultant, Julie worked with multiple organisations in computer systems validation and in the design and implementation of Quality Management Systems to international and local standards. Julie brings experience in the product development life cycle and the subsequent transition to commercial manufacture.