Mark has 25 years’ experience in cGMP compliant manufacturing, including 10 years in the development, set up and integration of a number of sterile and non-sterile pharmacy-based businesses operating to PIC/s standards.
Experience and a focus in project management has seen Mark deliver on five facility builds from concept, through regulatory approval and operational go live.
Mark currently leads a team of 400 operations, quality, regulatory, systems and facility staff. His continual focus on quality and continuous improvement has led to significant successes in business performance.